hereditary spastic paraplegia 4
hereditary spastic paraplegia that is characterized by slowly progressive muscle weakness and spasticity and has material basis in mutation in the SPAST gene on chromosome 2p22
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hereditary spastic paraplegia 4
Summary
hereditary spastic paraplegia 4 is a hereditary disorder[1].
Key Facts
- hereditary spastic paraplegia 4's instance of is recorded as hereditary disorder[2].
- hereditary spastic paraplegia 4's instance of is recorded as rare disease[3].
- hereditary spastic paraplegia 4's instance of is recorded as class of disease[4].
- hereditary spastic paraplegia 4's subclass of is recorded as hereditary spastic paraplegia[5].
- hereditary spastic paraplegia 4's subclass of is recorded as pure or complex autosomal dominant spastic paraplegia[6].
- hereditary spastic paraplegia 4's subclass of is recorded as autosomal dominant disease[7].
- hereditary spastic paraplegia 4's MeSH descriptor ID is recorded as C536865[8].
- hereditary spastic paraplegia 4's OMIM ID is recorded as 182601[9].
- hereditary spastic paraplegia 4's Disease Ontology ID is recorded as DOID:0110792[10].
- hereditary spastic paraplegia 4's Orphanet ID is recorded as 100985[11].
- hereditary spastic paraplegia 4's NCI Thesaurus ID is recorded as C129981[12].
- hereditary spastic paraplegia 4's health specialty is recorded as neurology[13].
- hereditary spastic paraplegia 4's genetic association is recorded as SPAST[14].
- hereditary spastic paraplegia 4's Google Knowledge Graph ID is recorded as /g/120vz17w[15].
- hereditary spastic paraplegia 4's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110792[16].
- hereditary spastic paraplegia 4's exact match is recorded as http://identifiers.org/doid/DOID:0110792[17].
- hereditary spastic paraplegia 4's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_100985[18].
- hereditary spastic paraplegia 4's UMLS CUI is recorded as C1866855[19].
- hereditary spastic paraplegia 4's ICD-10-CM is recorded as G11.4[20].
- hereditary spastic paraplegia 4's GARD rare disease ID is recorded as 4925[21].
- hereditary spastic paraplegia 4's on focus list of Wikimedia project is recorded as WikiProject Medicine[22].
- hereditary spastic paraplegia 4's Mondo ID is recorded as MONDO_0008438[23].
- hereditary spastic paraplegia 4's UniProt disease ID is recorded as DI-01036[24].