Werdnig–Hoffmann disease
Human disease
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Werdnig–Hoffmann disease
Summary
Werdnig–Hoffmann disease is a rare disease[1]. It is known by 19 alternative names across languages and contexts.[2]
Key Facts
- Werdnig–Hoffmann disease's instance of is recorded as rare disease[3].
- Werdnig–Hoffmann disease's instance of is recorded as neuromuscular disease[4].
- Werdnig–Hoffmann disease's instance of is recorded as class of disease[5].
- Guido Werdnig is named after Werdnig–Hoffmann disease[6].
- Johann Hoffmann is named after Werdnig–Hoffmann disease[7].
- Werdnig–Hoffmann disease is a type of survival motor neuron spinal muscular atrophy[8].
- Werdnig–Hoffmann disease's ICD-9-CM is recorded as 335.0[9].
- Werdnig–Hoffmann disease's NCI Thesaurus ID is recorded as C98670[10].
- Werdnig–Hoffmann disease's health specialty is recorded as neurology[11].
- Werdnig–Hoffmann disease's genetic association is recorded as SMN1[12].
- Werdnig–Hoffmann disease's exact match is recorded as http://purl.obolibrary.org/obo/DOID_13137[13].
- Werdnig–Hoffmann disease's exact match is recorded as http://identifiers.org/doid/DOID:13137[14].
- Werdnig–Hoffmann disease's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
Why It Matters
Werdnig–Hoffmann disease is known by 19 alternative names across languages and contexts.[2]