hereditary spastic paraplegia 31
30 years). In some cases, it can present as a complex phenotype with additional associated manifestations including peripheral neuropathy, bulbar palsy (with dysarthria and dysphagia), distal amyotrophy, and impaired distal vibration sense.
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Summary
hereditary spastic paraplegia 31 is a rare disease[1]. It draws 28 Wikipedia views per month (rare_disease category, ranking #237 of 627).[2]
Key Facts
- hereditary spastic paraplegia 31's instance of is recorded as rare disease[3].
- hereditary spastic paraplegia 31's instance of is recorded as class of disease[4].
- hereditary spastic paraplegia 31 is a type of hereditary spastic paraplegia[5].
- hereditary spastic paraplegia 31 is a type of pure or complex autosomal dominant spastic paraplegia[6].
- hereditary spastic paraplegia 31 is a type of autosomal dominant disease[7].
- hereditary spastic paraplegia 31's NCI Thesaurus ID is recorded as C189921[8].
- hereditary spastic paraplegia 31's health specialty is recorded as neurology[9].
- hereditary spastic paraplegia 31's genetic association is recorded as REEP1[10].
- hereditary spastic paraplegia 31's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110782[11].
- hereditary spastic paraplegia 31's exact match is recorded as http://identifiers.org/doid/DOID:0110782[12].
- hereditary spastic paraplegia 31's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_101011[13].
- hereditary spastic paraplegia 31's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
Why It Matters
hereditary spastic paraplegia 31 draws 28 Wikipedia views per month (rare_disease category, ranking #237 of 627).[2] It is known by 8 alternative names across languages and contexts.[15]