hereditary spastic paraplegia 13
hereditary spastic paraplegia that is characterized by a pure form of the disease with late onset and has material basis in mutation in the HSPD1 on chromosome 2q33
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hereditary spastic paraplegia 13
Summary
hereditary spastic paraplegia 13 is a rare disease[1].
Key Facts
- hereditary spastic paraplegia 13's instance of is recorded as rare disease[2].
- hereditary spastic paraplegia 13's instance of is recorded as class of disease[3].
- hereditary spastic paraplegia 13's subclass of is recorded as hereditary spastic paraplegia[4].
- hereditary spastic paraplegia 13's subclass of is recorded as pure or complex autosomal dominant spastic paraplegia[5].
- hereditary spastic paraplegia 13's subclass of is recorded as autosomal dominant disease[6].
- hereditary spastic paraplegia 13's MeSH descriptor ID is recorded as C537485[7].
- hereditary spastic paraplegia 13's OMIM ID is recorded as 605280[8].
- hereditary spastic paraplegia 13's Disease Ontology ID is recorded as DOID:0110766[9].
- hereditary spastic paraplegia 13's Orphanet ID is recorded as 100994[10].
- hereditary spastic paraplegia 13's health specialty is recorded as neurology[11].
- hereditary spastic paraplegia 13's genetic association is recorded as HSPD1[12].
- hereditary spastic paraplegia 13's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110766[13].
- hereditary spastic paraplegia 13's exact match is recorded as http://identifiers.org/doid/DOID:0110766[14].
- hereditary spastic paraplegia 13's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_100994[15].
- hereditary spastic paraplegia 13's UMLS CUI is recorded as C1854467[16].
- hereditary spastic paraplegia 13's ICD-10-CM is recorded as G11.4[17].
- hereditary spastic paraplegia 13's GARD rare disease ID is recorded as 9616[18].
- hereditary spastic paraplegia 13's on focus list of Wikimedia project is recorded as WikiProject Medicine[19].
- hereditary spastic paraplegia 13's Mondo ID is recorded as MONDO_0011532[20].
- hereditary spastic paraplegia 13's UniProt disease ID is recorded as DI-01039[21].