hereditary spastic paraplegia 30
hereditary spastic paraplegia that has material basis in mutation in the KIF1A gene on chromosome 2q37
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hereditary spastic paraplegia 30
Summary
hereditary spastic paraplegia 30 is a rare disease[1].
Key Facts
- hereditary spastic paraplegia 30's instance of is recorded as rare disease[2].
- hereditary spastic paraplegia 30's instance of is recorded as class of disease[3].
- hereditary spastic paraplegia 30's subclass of is recorded as hereditary spastic paraplegia[4].
- hereditary spastic paraplegia 30's subclass of is recorded as pure or complex autosomal recessive spastic paraplegia[5].
- hereditary spastic paraplegia 30's subclass of is recorded as pure or complex autosomal dominant spastic paraplegia[6].
- hereditary spastic paraplegia 30's subclass of is recorded as autosomal recessive disease[7].
- hereditary spastic paraplegia 30's MeSH descriptor ID is recorded as C563677[8].
- hereditary spastic paraplegia 30's OMIM ID is recorded as 610357[9].
- hereditary spastic paraplegia 30's Disease Ontology ID is recorded as DOID:0110781[10].
- hereditary spastic paraplegia 30's Orphanet ID is recorded as 101010[11].
- hereditary spastic paraplegia 30's NCI Thesaurus ID is recorded as C170435[12].
- hereditary spastic paraplegia 30's health specialty is recorded as neurology[13].
- hereditary spastic paraplegia 30's genetic association is recorded as KIF1A[14].
- hereditary spastic paraplegia 30's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110781[15].
- hereditary spastic paraplegia 30's exact match is recorded as http://identifiers.org/doid/DOID:0110781[16].
- hereditary spastic paraplegia 30's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_101010[17].
- hereditary spastic paraplegia 30's UMLS CUI is recorded as C1835896[18].
- hereditary spastic paraplegia 30's ICD-10-CM is recorded as G11.4[19].
- hereditary spastic paraplegia 30's on focus list of Wikimedia project is recorded as WikiProject Medicine[20].
- hereditary spastic paraplegia 30's Mondo ID is recorded as MONDO_0012476[21].
- hereditary spastic paraplegia 30's UniProt disease ID is recorded as DI-03243[22].