hereditary spastic paraplegia 30
hereditary spastic paraplegia that has material basis in mutation in the KIF1A gene on chromosome 2q37
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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 is a type of hereditary spastic paraplegia[4].
- hereditary spastic paraplegia 30 is a type of pure or complex autosomal recessive spastic paraplegia[5].
- hereditary spastic paraplegia 30 is a type of pure or complex autosomal dominant spastic paraplegia[6].
- hereditary spastic paraplegia 30 is a type of autosomal recessive disease[7].
- hereditary spastic paraplegia 30's NCI Thesaurus ID is recorded as C170435[8].
- hereditary spastic paraplegia 30's health specialty is recorded as neurology[9].
- hereditary spastic paraplegia 30's genetic association is recorded as KIF1A[10].
- hereditary spastic paraplegia 30's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110781[11].
- hereditary spastic paraplegia 30's exact match is recorded as http://identifiers.org/doid/DOID:0110781[12].
- hereditary spastic paraplegia 30's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_101010[13].
- hereditary spastic paraplegia 30's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].