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UMLS

Spastisk paraplegi, ärftlig

spastická paraplegie dědičná

C0037773    CZE (Czech)     MSHCZE (Medical Subject Headings Czech Language Edition )

Hereditární spastická paraplegie

C0037773    CZE (Czech)     MDRCZE (MedDRA Czech)

Strumpellova nemoc

C0037773    CZE (Czech)     MDRCZE (MedDRA Czech)

Hereditaire spastische paraplegie

C0037773    DUT (Dutch)     ICD10DUT (ICD10, Dutch Translation)

Hereditaire spastische paraplegie

C0037773    DUT (Dutch)     MSHDUT (Medical Subject Headings Dutch Language Edition )

Paraplegie, hereditaire spastische

C0037773    DUT (Dutch)     MSHDUT (Medical Subject Headings Dutch Language Edition )

Spastische paraplegie, hereditaire

C0037773    DUT (Dutch)     MSHDUT (Medical Subject Headings Dutch Language Edition )

congenitaal; paraplegie, spastisch

C0037773    DUT (Dutch)     ICPC2ICD10DUT (ICPC2-ICD10ENG Thesaurus Dutch)

familiaal; paralyse, spastisch

C0037773    DUT (Dutch)     ICPC2ICD10DUT (ICPC2-ICD10ENG Thesaurus Dutch)

paralyse; familiaal, spastisch

C0037773    DUT (Dutch)     ICPC2ICD10DUT (ICPC2-ICD10ENG Thesaurus Dutch)

paralyse; spastisch, familiaal

C0037773    DUT (Dutch)     ICPC2ICD10DUT (ICPC2-ICD10ENG Thesaurus Dutch)

paralyse; spastisch, hereditair

C0037773    DUT (Dutch)     ICPC2ICD10DUT (ICPC2-ICD10ENG Thesaurus Dutch)

paraplegie; spastisch, hereditair

C0037773    DUT (Dutch)     ICPC2ICD10DUT (ICPC2-ICD10ENG Thesaurus Dutch)

spastisch; paralyse, familiaal

C0037773    DUT (Dutch)     ICPC2ICD10DUT (ICPC2-ICD10ENG Thesaurus Dutch)

spastisch; paralyse, hereditair

C0037773    DUT (Dutch)     ICPC2ICD10DUT (ICPC2-ICD10ENG Thesaurus Dutch)

spastisch; paraplegie, hereditair

C0037773    DUT (Dutch)     ICPC2ICD10DUT (ICPC2-ICD10ENG Thesaurus Dutch)

spastische paraplegie, erfelijk

C0037773    DUT (Dutch)     MDRDUT (MedDRA Dutch)

ziekte van Strumpell

C0037773    DUT (Dutch)     MDRDUT (MedDRA Dutch)

Spastic Paraplegia, Hereditary

C0037773    ENG (English)     MSH (Medical Subject Headings )

Spastic Paraplegia, Hereditary

C0037773    ENG (English)     NDFRT (National Drug File - Reference Terminology)

Spastic Paraplegia, Hereditary

C0037773    ENG (English)     MTH (Metathesaurus Names )

Hereditary Spastic Paraplegia

C0037773    ENG (English)     NDFRT (National Drug File - Reference Terminology)

Hereditary Spastic Paraplegia

C0037773    ENG (English)     MSH (Medical Subject Headings )

Hereditary Spastic Paraplegias

C0037773    ENG (English)     MSH (Medical Subject Headings )

Paraplegia, Hereditary Spastic

C0037773    ENG (English)     MSH (Medical Subject Headings )

Paraplegia, Spastic, Hereditary

C0037773    ENG (English)     NDFRT (National Drug File - Reference Terminology)

Paraplegia, Spastic, Hereditary

C0037773    ENG (English)     MSH (Medical Subject Headings )

Paraplegias, Hereditary Spastic

C0037773    ENG (English)     MSH (Medical Subject Headings )

Spastic Paraplegias, Hereditary

C0037773    ENG (English)     MSH (Medical Subject Headings )

Hereditary spastic paraplegia

C0037773    ENG (English)     ICD10

Hereditary spastic paraplegia

C0037773    ENG (English)     ICD10AM

Hereditary spastic paraplegia

C0037773    ENG (English)     MDR (MedDRA)

Hereditary spastic paraplegia

C0037773    ENG (English)     RCD (Read Codes)

Hereditary spastic paraplegia

C0037773    ENG (English)     SNMI (SNOMED Intl )

Hereditary spastic paraplegia

C0037773    ENG (English)     ICD10CM

Hereditary spastic paraplegia

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

Hereditary spastic paraplegia

C0037773    ENG (English)     ICD9CM

Hereditary spastic paraplegia

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

PARAPLEGIA, SPASTIC HEREDITARY

C0037773    ENG (English)     DXP (DXplain)

hereditary spastic paraplegias

C0037773    ENG (English)     CHV

hereditary spastic paraplegia

C0037773    ENG (English)     CHV

spastic paraplegia hereditary

C0037773    ENG (English)     CHV

paraplegia; spastic, hereditary

C0037773    ENG (English)     ICPC2ICD10ENG

spastic; paraplegia, hereditary

C0037773    ENG (English)     ICPC2ICD10ENG

HMSN Type V

C0037773    ENG (English)     NDFRT (National Drug File - Reference Terminology)

HMSN Type V

C0037773    ENG (English)     MSH (Medical Subject Headings )

Type V, HMSN

C0037773    ENG (English)     MSH (Medical Subject Headings )

Spastic congenital paraplegia

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

PARAPLEGIA, SPASTIC CONGENITAL

C0037773    ENG (English)     DXP (DXplain)

congenital; paraplegia, spastic

C0037773    ENG (English)     ICPC2ICD10ENG

PARALYSIS, SPASTIC SPINAL FAMILIAL

C0037773    ENG (English)     DXP (DXplain)

PARAPLEGIA, SPASMODIC INFANTILE

C0037773    ENG (English)     DXP (DXplain)

Strumpell-Lorrain disease

C0037773    ENG (English)     SNM (SNOMED )

Strumpell-Lorrain disease

C0037773    ENG (English)     SNMI (SNOMED Intl )

Strumpell-Lorrain disease

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

Familial spastic paraplegia syndrome

C0037773    ENG (English)     SNM (SNOMED )

Familial spastic paraplegia syndrome

C0037773    ENG (English)     SNMI (SNOMED Intl )

Familial spastic paraplegia syndrome

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

Type V Hereditary Motor and Sensory Neuropathy

C0037773    ENG (English)     NDFRT (National Drug File - Reference Terminology)

Type V Hereditary Motor and Sensory Neuropathy

C0037773    ENG (English)     MSH (Medical Subject Headings )

Hereditary sensory-motor neuropathy, type V

C0037773    ENG (English)     SNMI (SNOMED Intl )

Hereditary sensory-motor neuropathy, type V

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

Hereditary motor and sensory neuropathy type V

C0037773    ENG (English)     RCD (Read Codes)

Hereditary motor and sensory neuropathy type V

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

Hereditary motor and sensory neuropathy, type V

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

Spastic paraplegia with hypertrophic sensory-motor neuropathy, type V

C0037773    ENG (English)     SNMI (SNOMED Intl )

Spastic paraplegia with hypertrophic sensory-motor neuropathy, type V

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

Strumpell disease

C0037773    ENG (English)     RCD (Read Codes)

Strumpell disease

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

strumpell`s disease

C0037773    ENG (English)     CHV

Strumpell`s disease

C0037773    ENG (English)     MDR (MedDRA)

Hered mtr/sen neurop & pyr sgn

C0037773    ENG (English)     RCD (Read Codes)

HSP - Heredit spast paraplegia

C0037773    ENG (English)     RCD (Read Codes)

Heredit motr/sens neuropathy V

C0037773    ENG (English)     RCD (Read Codes)

HSP - Hereditary spastic paraplegia

C0037773    ENG (English)     RCD (Read Codes)

HSP - Hereditary spastic paraplegia

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

Hereditary Motor-Sensory Neuropathy with Pyramidal Signs

C0037773    ENG (English)     NDFRT (National Drug File - Reference Terminology)

Hereditary Motor-Sensory Neuropathy with Pyramidal Signs

C0037773    ENG (English)     MSH (Medical Subject Headings )

Hereditary motor-sensory neuropathy with pyramidal signs

C0037773    ENG (English)     RCD (Read Codes)

Hereditary motor-sensory neuropathy with pyramidal signs

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

Hereditary Motor Sensory Neuropathy with Pyramidal Signs

C0037773    ENG (English)     MSH (Medical Subject Headings )

Hereditary sensory-motor neuropathy, type 5

C0037773    ENG (English)     SNM (SNOMED )

Spastic paraplegia with hypertrophic motor-sensory neuropathy, type 5

C0037773    ENG (English)     SNM (SNOMED )

HMSN V (Hereditary Motor and Sensory Neuropathy Type V)

C0037773    ENG (English)     NDFRT (National Drug File - Reference Terminology)

HMSN V (Hereditary Motor and Sensory Neuropathy Type V)

C0037773    ENG (English)     MSH (Medical Subject Headings )

Spastic Paraplegia-Hypertrophic Motor-Sensory Neuropathy

C0037773    ENG (English)     NDFRT (National Drug File - Reference Terminology)

Spastic Paraplegia-Hypertrophic Motor-Sensory Neuropathy

C0037773    ENG (English)     MSH (Medical Subject Headings )

Hypertrophic Motor-Sensory Neuropathy-Spastic Paraplegia

C0037773    ENG (English)     NDFRT (National Drug File - Reference Terminology)

Hypertrophic Motor-Sensory Neuropathy-Spastic Paraplegia

C0037773    ENG (English)     MSH (Medical Subject Headings )

Hypertrophic Motor Sensory Neuropathy Spastic Paraplegia

C0037773    ENG (English)     MSH (Medical Subject Headings )

Spastic Paraplegia Hypertrophic Motor Sensory Neuropathy

C0037773    ENG (English)     MSH (Medical Subject Headings )

Hereditary sensory-motor neuropathy, type V (disorder)

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

Hereditary spastic paraplegia (disorder)

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

HMSN V

C0037773    ENG (English)     OMIM

HMSN V

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

HSMN V

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

spastic; paralysis, familial

C0037773    ENG (English)     ICPC2ICD10ENG

familial; paralysis, spastic

C0037773    ENG (English)     ICPC2ICD10ENG

paralysis; familial, spastic

C0037773    ENG (English)     ICPC2ICD10ENG

paralysis; spastic, familial

C0037773    ENG (English)     ICPC2ICD10ENG

spastic; paralysis, hereditary

C0037773    ENG (English)     ICPC2ICD10ENG

paralysis; spastic, hereditary

C0037773    ENG (English)     ICPC2ICD10ENG

Hered spastic paraplegia

C0037773    ENG (English)     ICD9CM

HEREDITARY MOTOR AND SENSORY NEUROPATHY V

C0037773    ENG (English)     OMIM

CMT WITH PYRAMIDAL FEATURES

C0037773    ENG (English)     OMIM

HMSN5

C0037773    ENG (English)     OMIM

familial spastic paraplegia (diagnosis)

C0037773    ENG (English)     MEDCIN

familial spastic paraplegia

C0037773    ENG (English)     MEDCIN

Spastic Paraplegia, Hereditary [Disease/Finding]

C0037773    ENG (English)     NDFRT (National Drug File - Reference Terminology)

HMSN 5

C0037773    ENG (English)     NDFRT (National Drug File - Reference Terminology)

HMSN 5

C0037773    ENG (English)     MSH (Medical Subject Headings )

Hereditary Motor and Sensory Neuropathy 5

C0037773    ENG (English)     NDFRT (National Drug File - Reference Terminology)

Hereditary Motor and Sensory Neuropathy 5

C0037773    ENG (English)     MSH (Medical Subject Headings )

Perinnöllinen spastinen paraplegia

C0037773    FIN (Finnish)     MSHFIN (Medical Subject Headings Finnish Language Edition )

Paraplégie spasmodique héréditaire

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Paraplégie spastique héréditaire

C0037773    FRE (French)     MDRFRE (MedDRA French)

Paraplégie spastique héréditaire

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Neuropathie sensitivo-motrice héréditaire de type 5

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Neuropathie sensitivo-motrice héréditaire de type V

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Neuropathie sensitivomotrice héréditaire de type 5

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Neuropathie sensitivomotrice héréditaire de type V

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Maladie de Strümpell-Lorrain

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

NHMS de type 5

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

NHMS de type V

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Neuropathie héréditaire motrice et sensitive de type 5

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Neuropathie héréditaire motrice et sensitive de type V

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Neuropathie héréditaire motrice et sensorielle de type V

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Paraparésie spasmodique

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Paraplégie spastique familiale

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Maladie de Strumpell

C0037773    FRE (French)     MDRFRE (MedDRA French)

NMSH de type V

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Neuropathie motrice et sensitive héréditaire de type V

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

NMSH de type 5

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Spastische Paraplegie, hereditäre

C0037773    GER (German)     MSHGER (Medical Subject Headings German Language Edition )

HMSN Typ V

C0037773    GER (German)     MSHGER (Medical Subject Headings German Language Edition )

Hereditaere spastische Paraplegie

C0037773    GER (German)     DMDICD10 (ICD-10 German)

Hereditäre spastische Paraplegie

C0037773    GER (German)     MSHGER (Medical Subject Headings German Language Edition )

Paraplegie, spastische, hereditäre

C0037773    GER (German)     MSHGER (Medical Subject Headings German Language Edition )

hereditaere spastische Paraplegie

C0037773    GER (German)     MDRGER (MedDRA German)

Struempell-Krankheit

C0037773    GER (German)     MDRGER (MedDRA German)

Veleszületett spasticus paraplegia

C0037773    HUN (Hungarian)     MDRHUN (MedDRA Hungarian)

Strumpell-betegség

C0037773    HUN (Hungarian)     MDRHUN (MedDRA Hungarian)

Paraplegia spastica ereditaria

C0037773    ITA (Italian)     MDRITA (MedDRA Italian)

Paraplegia spastica ereditaria

C0037773    ITA (Italian)     MSHITA (Medical Subject Headings Italian Language Edition )

Malattia di Strumpell

C0037773    ITA (Italian)     MDRITA (MedDRA Italian)

HMSN tipo V

C0037773    ITA (Italian)     MSHITA (Medical Subject Headings Italian Language Edition )

HMSN V (neuropatia ereditaria sensitivo-motoria tipo V)

C0037773    ITA (Italian)     MSHITA (Medical Subject Headings Italian Language Edition )

Neuropatia ereditaria sensitivo-motoria con segni piramidali

C0037773    ITA (Italian)     MSHITA (Medical Subject Headings Italian Language Edition )

Neuropatia ereditaria sensitivo-motoria tipo V

C0037773    ITA (Italian)     MSHITA (Medical Subject Headings Italian Language Edition )

Neuropatia ipertrofica sensitivo-motoria associata a paraplegia spastica

C0037773    ITA (Italian)     MSHITA (Medical Subject Headings Italian Language Edition )

HMSN-V型

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

ニューロパチー-遺伝性運動感覚性V型

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

ニューロパチー-遺伝性運動感覚性5型

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

遺伝性運動感覚性ニューロパチー5型

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

遺伝性運動感覚性ニューロパチーV型

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

HMSN5型

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

家族性強直性対麻痺

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

強直性対麻痺-遺伝性

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

痙性脊髄麻痺

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

進行性強直性対麻痺

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

遺伝性強直性対麻痺

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

遺伝性痙性対麻痺

C0037773    JPN (Japanese)     MDRJPN (MedDRA Japanese)

遺伝性痙性対麻痺

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

シュトリュンペルビョウ

C0037773    JPN (Japanese)     MDRJPN (MedDRA Japanese)

シュトリュンペル病

C0037773    JPN (Japanese)     MDRJPN (MedDRA Japanese)

イデンセイケイセイツイマヒ

C0037773    JPN (Japanese)     MDRJPN (MedDRA Japanese)

遺伝性運動感覚性ニューロパシー5型

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

ニューロパシー-遺伝性運動感覚性5型

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

家族性痙性対麻痺

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

対麻痺-強直性-遺伝性

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

遺伝性運動感覚性ニューロパシーV型

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

対麻痺-遺伝性痙性

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

痙性対麻痺-遺伝性

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

유전성 강직성 대마비

C0037773    KOR (Korean)     KCD5

Arvelig spastisk paraplegi

C0037773    NOR (Norwegian)     MSHNOR

Strümpel-Lorrains sykdom

C0037773    NOR (Norwegian)     MSHNOR

Hereditær spastisk paraplegi

C0037773    NOR (Norwegian)     MSHNOR

Porażenie połowicze spastyczne wrodzone

C0037773    POL (Polish)     MSHPOL (Medical Subject Headings Polish Language Edition )

Dziedziczna paraplegia spastyczna

C0037773    POL (Polish)     MSHPOL (Medical Subject Headings Polish Language Edition )

Paraplegia spastyczna wrodzona

C0037773    POL (Polish)     MSHPOL (Medical Subject Headings Polish Language Edition )

Spastyczne wrodzone porażenie połowicze

C0037773    POL (Polish)     MSHPOL (Medical Subject Headings Polish Language Edition )

Paraplegia Espástica Hereditária

C0037773    POR (Portuguese)     MSHPOR (Medical Subject Headings Portuguese Language Edition )

Paraplegia Espástica Hereditária Ligada ao X

C0037773    POR (Portuguese)     MSHPOR (Medical Subject Headings Portuguese Language Edition )

Doença de Strumpell

C0037773    POR (Portuguese)     MDRPOR (MedDRA Portuguese)

Paraplegia espástica hereditária

C0037773    POR (Portuguese)     MDRPOR (MedDRA Portuguese)

СПАСТИЧЕСКАЯ ПАРАПЛЕГИЯ НАСЛЕДСТВЕННАЯ

C0037773    RUS (Russian)     MSHRUS (Medical Subject Headings Russian Language Edition )

SPASTICHESKAIA PARAPLEGIIA NASLEDSTVENNAIA

C0037773    RUS (Russian)     MSHRUS (Medical Subject Headings Russian Language Edition )

HMSN TIP V

C0037773    RUS (Russian)     MSHRUS (Medical Subject Headings Russian Language Edition )

NASLEDSTVENNAIA SPASTICHESKAIA PARAPLEGIIA

C0037773    RUS (Russian)     MSHRUS (Medical Subject Headings Russian Language Edition )

PARAPLEGIIA SPASTICHESKAIA NASLEDSTVENNAIA

C0037773    RUS (Russian)     MSHRUS (Medical Subject Headings Russian Language Edition )

SHTRIUMPELIA SPASTICHESKAIA PARAPLEGIIA

C0037773    RUS (Russian)     MSHRUS (Medical Subject Headings Russian Language Edition )

HMSN ТИП V

C0037773    RUS (Russian)     MSHRUS (Medical Subject Headings Russian Language Edition )

НАСЛЕДСТВЕННАЯ СПАСТИЧЕСКАЯ ПАРАПЛЕГИЯ

C0037773    RUS (Russian)     MSHRUS (Medical Subject Headings Russian Language Edition )

ПАРАПЛЕГИЯ СПАСТИЧЕСКАЯ НАСЛЕДСТВЕННАЯ

C0037773    RUS (Russian)     MSHRUS (Medical Subject Headings Russian Language Edition )

ШТРЮМПЕЛЯ СПАСТИЧЕСКАЯ ПАРАПЛЕГИЯ

C0037773    RUS (Russian)     MSHRUS (Medical Subject Headings Russian Language Edition )

neuropatía sensitivomotora hereditaria, tipo V

C0037773    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

Enfermedad de Strumpell

C0037773    SPA (Spanish)     MDRSPA (MedDRA Spanish)

enfermedad de Strumpell - Lorrain

C0037773    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

neuropatía sensitivomotora hereditaria, tipo V (trastorno)

C0037773    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

paraplejía espástica con neuropatía sensitivomotora hipertrófica, tipo V

C0037773    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

paraplejía espástica hereditaria

C0037773    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

paraplejía espástica hereditaria (trastorno)

C0037773    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

síndrome de paraplejía espástica familiar

C0037773    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

Paraplejia espástica hereditaria

C0037773    SPA (Spanish)     MDRSPA (MedDRA Spanish)

Hereditary spastic paraplegia

C0037773    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

Paraplejía Espástica Hereditaria

C0037773    SPA (Spanish)     MSHSPA (Medical Subject Headings Spanish Language Edition )

Paraplejía Espástica Hereditaria Ligada al X

C0037773    SPA (Spanish)     MSHSPA (Medical Subject Headings Spanish Language Edition )

Spastisk paraplegi, ärftlig

C0037773    SWE (Swedish)     MSHSWE (Medical Subject Headings Swedish Language Edition )

spastická paraplegie dědičná

C0037773    CZE (Czech)     MSHCZE (Medical Subject Headings Czech Language Edition )

Hereditární spastická paraplegie

C0037773    CZE (Czech)     MDRCZE (MedDRA Czech)

Strumpellova nemoc

C0037773    CZE (Czech)     MDRCZE (MedDRA Czech)

Hereditaire spastische paraplegie

C0037773    DUT (Dutch)     ICD10DUT (ICD10, Dutch Translation)

Hereditaire spastische paraplegie

C0037773    DUT (Dutch)     MSHDUT (Medical Subject Headings Dutch Language Edition )

Paraplegie, hereditaire spastische

C0037773    DUT (Dutch)     MSHDUT (Medical Subject Headings Dutch Language Edition )

Spastische paraplegie, hereditaire

C0037773    DUT (Dutch)     MSHDUT (Medical Subject Headings Dutch Language Edition )

congenitaal; paraplegie, spastisch

C0037773    DUT (Dutch)     ICPC2ICD10DUT (ICPC2-ICD10ENG Thesaurus Dutch)

familiaal; paralyse, spastisch

C0037773    DUT (Dutch)     ICPC2ICD10DUT (ICPC2-ICD10ENG Thesaurus Dutch)

paralyse; familiaal, spastisch

C0037773    DUT (Dutch)     ICPC2ICD10DUT (ICPC2-ICD10ENG Thesaurus Dutch)

paralyse; spastisch, familiaal

C0037773    DUT (Dutch)     ICPC2ICD10DUT (ICPC2-ICD10ENG Thesaurus Dutch)

paralyse; spastisch, hereditair

C0037773    DUT (Dutch)     ICPC2ICD10DUT (ICPC2-ICD10ENG Thesaurus Dutch)

paraplegie; spastisch, hereditair

C0037773    DUT (Dutch)     ICPC2ICD10DUT (ICPC2-ICD10ENG Thesaurus Dutch)

spastisch; paralyse, familiaal

C0037773    DUT (Dutch)     ICPC2ICD10DUT (ICPC2-ICD10ENG Thesaurus Dutch)

spastisch; paralyse, hereditair

C0037773    DUT (Dutch)     ICPC2ICD10DUT (ICPC2-ICD10ENG Thesaurus Dutch)

spastisch; paraplegie, hereditair

C0037773    DUT (Dutch)     ICPC2ICD10DUT (ICPC2-ICD10ENG Thesaurus Dutch)

spastische paraplegie, erfelijk

C0037773    DUT (Dutch)     MDRDUT (MedDRA Dutch)

ziekte van Strumpell

C0037773    DUT (Dutch)     MDRDUT (MedDRA Dutch)

Spastic Paraplegia, Hereditary

C0037773    ENG (English)     MSH (Medical Subject Headings )

Spastic Paraplegia, Hereditary

C0037773    ENG (English)     NDFRT (National Drug File - Reference Terminology)

Spastic Paraplegia, Hereditary

C0037773    ENG (English)     MTH (Metathesaurus Names )

Hereditary Spastic Paraplegia

C0037773    ENG (English)     NDFRT (National Drug File - Reference Terminology)

Hereditary Spastic Paraplegia

C0037773    ENG (English)     MSH (Medical Subject Headings )

Hereditary Spastic Paraplegias

C0037773    ENG (English)     MSH (Medical Subject Headings )

Paraplegia, Hereditary Spastic

C0037773    ENG (English)     MSH (Medical Subject Headings )

Paraplegia, Spastic, Hereditary

C0037773    ENG (English)     NDFRT (National Drug File - Reference Terminology)

Paraplegia, Spastic, Hereditary

C0037773    ENG (English)     MSH (Medical Subject Headings )

Paraplegias, Hereditary Spastic

C0037773    ENG (English)     MSH (Medical Subject Headings )

Spastic Paraplegias, Hereditary

C0037773    ENG (English)     MSH (Medical Subject Headings )

Hereditary spastic paraplegia

C0037773    ENG (English)     ICD10

Hereditary spastic paraplegia

C0037773    ENG (English)     ICD10AM

Hereditary spastic paraplegia

C0037773    ENG (English)     MDR (MedDRA)

Hereditary spastic paraplegia

C0037773    ENG (English)     RCD (Read Codes)

Hereditary spastic paraplegia

C0037773    ENG (English)     SNMI (SNOMED Intl )

Hereditary spastic paraplegia

C0037773    ENG (English)     ICD10CM

Hereditary spastic paraplegia

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

Hereditary spastic paraplegia

C0037773    ENG (English)     ICD9CM

Hereditary spastic paraplegia

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

PARAPLEGIA, SPASTIC HEREDITARY

C0037773    ENG (English)     DXP (DXplain)

hereditary spastic paraplegias

C0037773    ENG (English)     CHV

hereditary spastic paraplegia

C0037773    ENG (English)     CHV

spastic paraplegia hereditary

C0037773    ENG (English)     CHV

paraplegia; spastic, hereditary

C0037773    ENG (English)     ICPC2ICD10ENG

spastic; paraplegia, hereditary

C0037773    ENG (English)     ICPC2ICD10ENG

HMSN Type V

C0037773    ENG (English)     NDFRT (National Drug File - Reference Terminology)

HMSN Type V

C0037773    ENG (English)     MSH (Medical Subject Headings )

Type V, HMSN

C0037773    ENG (English)     MSH (Medical Subject Headings )

Spastic congenital paraplegia

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

PARAPLEGIA, SPASTIC CONGENITAL

C0037773    ENG (English)     DXP (DXplain)

congenital; paraplegia, spastic

C0037773    ENG (English)     ICPC2ICD10ENG

PARALYSIS, SPASTIC SPINAL FAMILIAL

C0037773    ENG (English)     DXP (DXplain)

PARAPLEGIA, SPASMODIC INFANTILE

C0037773    ENG (English)     DXP (DXplain)

Strumpell-Lorrain disease

C0037773    ENG (English)     SNM (SNOMED )

Strumpell-Lorrain disease

C0037773    ENG (English)     SNMI (SNOMED Intl )

Strumpell-Lorrain disease

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

Familial spastic paraplegia syndrome

C0037773    ENG (English)     SNM (SNOMED )

Familial spastic paraplegia syndrome

C0037773    ENG (English)     SNMI (SNOMED Intl )

Familial spastic paraplegia syndrome

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

Type V Hereditary Motor and Sensory Neuropathy

C0037773    ENG (English)     NDFRT (National Drug File - Reference Terminology)

Type V Hereditary Motor and Sensory Neuropathy

C0037773    ENG (English)     MSH (Medical Subject Headings )

Hereditary sensory-motor neuropathy, type V

C0037773    ENG (English)     SNMI (SNOMED Intl )

Hereditary sensory-motor neuropathy, type V

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

Hereditary motor and sensory neuropathy type V

C0037773    ENG (English)     RCD (Read Codes)

Hereditary motor and sensory neuropathy type V

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

Hereditary motor and sensory neuropathy, type V

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

Spastic paraplegia with hypertrophic sensory-motor neuropathy, type V

C0037773    ENG (English)     SNMI (SNOMED Intl )

Spastic paraplegia with hypertrophic sensory-motor neuropathy, type V

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

Strumpell disease

C0037773    ENG (English)     RCD (Read Codes)

Strumpell disease

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

strumpell`s disease

C0037773    ENG (English)     CHV

Strumpell`s disease

C0037773    ENG (English)     MDR (MedDRA)

Hered mtr/sen neurop & pyr sgn

C0037773    ENG (English)     RCD (Read Codes)

HSP - Heredit spast paraplegia

C0037773    ENG (English)     RCD (Read Codes)

Heredit motr/sens neuropathy V

C0037773    ENG (English)     RCD (Read Codes)

HSP - Hereditary spastic paraplegia

C0037773    ENG (English)     RCD (Read Codes)

HSP - Hereditary spastic paraplegia

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

Hereditary Motor-Sensory Neuropathy with Pyramidal Signs

C0037773    ENG (English)     NDFRT (National Drug File - Reference Terminology)

Hereditary Motor-Sensory Neuropathy with Pyramidal Signs

C0037773    ENG (English)     MSH (Medical Subject Headings )

Hereditary motor-sensory neuropathy with pyramidal signs

C0037773    ENG (English)     RCD (Read Codes)

Hereditary motor-sensory neuropathy with pyramidal signs

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

Hereditary Motor Sensory Neuropathy with Pyramidal Signs

C0037773    ENG (English)     MSH (Medical Subject Headings )

Hereditary sensory-motor neuropathy, type 5

C0037773    ENG (English)     SNM (SNOMED )

Spastic paraplegia with hypertrophic motor-sensory neuropathy, type 5

C0037773    ENG (English)     SNM (SNOMED )

HMSN V (Hereditary Motor and Sensory Neuropathy Type V)

C0037773    ENG (English)     NDFRT (National Drug File - Reference Terminology)

HMSN V (Hereditary Motor and Sensory Neuropathy Type V)

C0037773    ENG (English)     MSH (Medical Subject Headings )

Spastic Paraplegia-Hypertrophic Motor-Sensory Neuropathy

C0037773    ENG (English)     NDFRT (National Drug File - Reference Terminology)

Spastic Paraplegia-Hypertrophic Motor-Sensory Neuropathy

C0037773    ENG (English)     MSH (Medical Subject Headings )

Hypertrophic Motor-Sensory Neuropathy-Spastic Paraplegia

C0037773    ENG (English)     NDFRT (National Drug File - Reference Terminology)

Hypertrophic Motor-Sensory Neuropathy-Spastic Paraplegia

C0037773    ENG (English)     MSH (Medical Subject Headings )

Hypertrophic Motor Sensory Neuropathy Spastic Paraplegia

C0037773    ENG (English)     MSH (Medical Subject Headings )

Spastic Paraplegia Hypertrophic Motor Sensory Neuropathy

C0037773    ENG (English)     MSH (Medical Subject Headings )

Hereditary sensory-motor neuropathy, type V (disorder)

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

Hereditary spastic paraplegia (disorder)

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

HMSN V

C0037773    ENG (English)     OMIM

HMSN V

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

HSMN V

C0037773    ENG (English)     SNM (SNOMED Clinical Terms )

spastic; paralysis, familial

C0037773    ENG (English)     ICPC2ICD10ENG

familial; paralysis, spastic

C0037773    ENG (English)     ICPC2ICD10ENG

paralysis; familial, spastic

C0037773    ENG (English)     ICPC2ICD10ENG

paralysis; spastic, familial

C0037773    ENG (English)     ICPC2ICD10ENG

spastic; paralysis, hereditary

C0037773    ENG (English)     ICPC2ICD10ENG

paralysis; spastic, hereditary

C0037773    ENG (English)     ICPC2ICD10ENG

Hered spastic paraplegia

C0037773    ENG (English)     ICD9CM

HEREDITARY MOTOR AND SENSORY NEUROPATHY V

C0037773    ENG (English)     OMIM

CMT WITH PYRAMIDAL FEATURES

C0037773    ENG (English)     OMIM

HMSN5

C0037773    ENG (English)     OMIM

familial spastic paraplegia (diagnosis)

C0037773    ENG (English)     MEDCIN

familial spastic paraplegia

C0037773    ENG (English)     MEDCIN

Spastic Paraplegia, Hereditary [Disease/Finding]

C0037773    ENG (English)     NDFRT (National Drug File - Reference Terminology)

HMSN 5

C0037773    ENG (English)     NDFRT (National Drug File - Reference Terminology)

HMSN 5

C0037773    ENG (English)     MSH (Medical Subject Headings )

Hereditary Motor and Sensory Neuropathy 5

C0037773    ENG (English)     NDFRT (National Drug File - Reference Terminology)

Hereditary Motor and Sensory Neuropathy 5

C0037773    ENG (English)     MSH (Medical Subject Headings )

Perinnöllinen spastinen paraplegia

C0037773    FIN (Finnish)     MSHFIN (Medical Subject Headings Finnish Language Edition )

Paraplégie spasmodique héréditaire

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Paraplégie spastique héréditaire

C0037773    FRE (French)     MDRFRE (MedDRA French)

Paraplégie spastique héréditaire

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Neuropathie sensitivo-motrice héréditaire de type 5

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Neuropathie sensitivo-motrice héréditaire de type V

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Neuropathie sensitivomotrice héréditaire de type 5

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Neuropathie sensitivomotrice héréditaire de type V

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Maladie de Strümpell-Lorrain

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

NHMS de type 5

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

NHMS de type V

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Neuropathie héréditaire motrice et sensitive de type 5

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Neuropathie héréditaire motrice et sensitive de type V

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Neuropathie héréditaire motrice et sensorielle de type V

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Paraparésie spasmodique

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Paraplégie spastique familiale

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Maladie de Strumpell

C0037773    FRE (French)     MDRFRE (MedDRA French)

NMSH de type V

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Neuropathie motrice et sensitive héréditaire de type V

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

NMSH de type 5

C0037773    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Spastische Paraplegie, hereditäre

C0037773    GER (German)     MSHGER (Medical Subject Headings German Language Edition )

HMSN Typ V

C0037773    GER (German)     MSHGER (Medical Subject Headings German Language Edition )

Hereditaere spastische Paraplegie

C0037773    GER (German)     DMDICD10 (ICD-10 German)

Hereditäre spastische Paraplegie

C0037773    GER (German)     MSHGER (Medical Subject Headings German Language Edition )

Paraplegie, spastische, hereditäre

C0037773    GER (German)     MSHGER (Medical Subject Headings German Language Edition )

hereditaere spastische Paraplegie

C0037773    GER (German)     MDRGER (MedDRA German)

Struempell-Krankheit

C0037773    GER (German)     MDRGER (MedDRA German)

Veleszületett spasticus paraplegia

C0037773    HUN (Hungarian)     MDRHUN (MedDRA Hungarian)

Strumpell-betegség

C0037773    HUN (Hungarian)     MDRHUN (MedDRA Hungarian)

Paraplegia spastica ereditaria

C0037773    ITA (Italian)     MDRITA (MedDRA Italian)

Paraplegia spastica ereditaria

C0037773    ITA (Italian)     MSHITA (Medical Subject Headings Italian Language Edition )

Malattia di Strumpell

C0037773    ITA (Italian)     MDRITA (MedDRA Italian)

HMSN tipo V

C0037773    ITA (Italian)     MSHITA (Medical Subject Headings Italian Language Edition )

HMSN V (neuropatia ereditaria sensitivo-motoria tipo V)

C0037773    ITA (Italian)     MSHITA (Medical Subject Headings Italian Language Edition )

Neuropatia ereditaria sensitivo-motoria con segni piramidali

C0037773    ITA (Italian)     MSHITA (Medical Subject Headings Italian Language Edition )

Neuropatia ereditaria sensitivo-motoria tipo V

C0037773    ITA (Italian)     MSHITA (Medical Subject Headings Italian Language Edition )

Neuropatia ipertrofica sensitivo-motoria associata a paraplegia spastica

C0037773    ITA (Italian)     MSHITA (Medical Subject Headings Italian Language Edition )

HMSN-V型

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

ニューロパチー-遺伝性運動感覚性V型

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

ニューロパチー-遺伝性運動感覚性5型

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

遺伝性運動感覚性ニューロパチー5型

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

遺伝性運動感覚性ニューロパチーV型

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

HMSN5型

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

家族性強直性対麻痺

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

強直性対麻痺-遺伝性

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

痙性脊髄麻痺

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

進行性強直性対麻痺

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

遺伝性強直性対麻痺

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

遺伝性痙性対麻痺

C0037773    JPN (Japanese)     MDRJPN (MedDRA Japanese)

遺伝性痙性対麻痺

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

シュトリュンペルビョウ

C0037773    JPN (Japanese)     MDRJPN (MedDRA Japanese)

シュトリュンペル病

C0037773    JPN (Japanese)     MDRJPN (MedDRA Japanese)

イデンセイケイセイツイマヒ

C0037773    JPN (Japanese)     MDRJPN (MedDRA Japanese)

遺伝性運動感覚性ニューロパシー5型

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

ニューロパシー-遺伝性運動感覚性5型

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

家族性痙性対麻痺

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

対麻痺-強直性-遺伝性

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

遺伝性運動感覚性ニューロパシーV型

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

対麻痺-遺伝性痙性

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

痙性対麻痺-遺伝性

C0037773    JPN (Japanese)     MSHJPN (Medical Subject Headings Japanese Language Edition )

유전성 강직성 대마비

C0037773    KOR (Korean)     KCD5

Arvelig spastisk paraplegi

C0037773    NOR (Norwegian)     MSHNOR

Strümpel-Lorrains sykdom

C0037773    NOR (Norwegian)     MSHNOR

Hereditær spastisk paraplegi

C0037773    NOR (Norwegian)     MSHNOR

Porażenie połowicze spastyczne wrodzone

C0037773    POL (Polish)     MSHPOL (Medical Subject Headings Polish Language Edition )

Dziedziczna paraplegia spastyczna

C0037773    POL (Polish)     MSHPOL (Medical Subject Headings Polish Language Edition )

Paraplegia spastyczna wrodzona

C0037773    POL (Polish)     MSHPOL (Medical Subject Headings Polish Language Edition )

Spastyczne wrodzone porażenie połowicze

C0037773    POL (Polish)     MSHPOL (Medical Subject Headings Polish Language Edition )

Paraplegia Espástica Hereditária

C0037773    POR (Portuguese)     MSHPOR (Medical Subject Headings Portuguese Language Edition )

Paraplegia Espástica Hereditária Ligada ao X

C0037773    POR (Portuguese)     MSHPOR (Medical Subject Headings Portuguese Language Edition )

Doença de Strumpell

C0037773    POR (Portuguese)     MDRPOR (MedDRA Portuguese)

Paraplegia espástica hereditária

C0037773    POR (Portuguese)     MDRPOR (MedDRA Portuguese)

СПАСТИЧЕСКАЯ ПАРАПЛЕГИЯ НАСЛЕДСТВЕННАЯ

C0037773    RUS (Russian)     MSHRUS (Medical Subject Headings Russian Language Edition )

SPASTICHESKAIA PARAPLEGIIA NASLEDSTVENNAIA

C0037773    RUS (Russian)     MSHRUS (Medical Subject Headings Russian Language Edition )

HMSN TIP V

C0037773    RUS (Russian)     MSHRUS (Medical Subject Headings Russian Language Edition )

NASLEDSTVENNAIA SPASTICHESKAIA PARAPLEGIIA

C0037773    RUS (Russian)     MSHRUS (Medical Subject Headings Russian Language Edition )

PARAPLEGIIA SPASTICHESKAIA NASLEDSTVENNAIA

C0037773    RUS (Russian)     MSHRUS (Medical Subject Headings Russian Language Edition )

SHTRIUMPELIA SPASTICHESKAIA PARAPLEGIIA

C0037773    RUS (Russian)     MSHRUS (Medical Subject Headings Russian Language Edition )

HMSN ТИП V

C0037773    RUS (Russian)     MSHRUS (Medical Subject Headings Russian Language Edition )

НАСЛЕДСТВЕННАЯ СПАСТИЧЕСКАЯ ПАРАПЛЕГИЯ

C0037773    RUS (Russian)     MSHRUS (Medical Subject Headings Russian Language Edition )

ПАРАПЛЕГИЯ СПАСТИЧЕСКАЯ НАСЛЕДСТВЕННАЯ

C0037773    RUS (Russian)     MSHRUS (Medical Subject Headings Russian Language Edition )

ШТРЮМПЕЛЯ СПАСТИЧЕСКАЯ ПАРАПЛЕГИЯ

C0037773    RUS (Russian)     MSHRUS (Medical Subject Headings Russian Language Edition )

neuropatía sensitivomotora hereditaria, tipo V

C0037773    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

Enfermedad de Strumpell

C0037773    SPA (Spanish)     MDRSPA (MedDRA Spanish)

enfermedad de Strumpell - Lorrain

C0037773    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

neuropatía sensitivomotora hereditaria, tipo V (trastorno)

C0037773    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

paraplejía espástica con neuropatía sensitivomotora hipertrófica, tipo V

C0037773    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

paraplejía espástica hereditaria

C0037773    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

paraplejía espástica hereditaria (trastorno)

C0037773    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

síndrome de paraplejía espástica familiar

C0037773    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

Paraplejia espástica hereditaria

C0037773    SPA (Spanish)     MDRSPA (MedDRA Spanish)

Hereditary spastic paraplegia

C0037773    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

Paraplejía Espástica Hereditaria

C0037773    SPA (Spanish)     MSHSPA (Medical Subject Headings Spanish Language Edition )

Paraplejía Espástica Hereditaria Ligada al X

C0037773    SPA (Spanish)     MSHSPA (Medical Subject Headings Spanish Language Edition )

Spastisk paraplegi, ärftlig

C0037773    SWE (Swedish)     MSHSWE (Medical Subject Headings Swedish Language Edition )


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