(Q5160420)

English

Congenital distal spinal muscular atrophy

hereditary condition characterized by muscle wasting

In more languages

Statements

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class of disease

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Distal hereditary motor neuropathies

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genetic association

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Alterations in the ankyrin domain of TRPV4 cause congenital distal SMA, scapuloperoneal SMA and HMSN2C

Identifiers

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Medical Dictionary for Regulatory Activities ID

1 reference

https://cdn.who.int/media/docs/default-source/classification/icd/icd-10/icd-10-to-meddra-map---june-2023---codes-mapping.xlsx

based on heuristic

inferred by common ICD-10 mappings on Wikidata and on source

Microsoft Academic ID

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1 reference

imported from Wikimedia project

English Wikipedia

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WikiProjectMed ID

Congenital distal spinal muscular atrophy

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Sitelinks

Wikipedia(2 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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