hereditary spastic paraplegia 10
hereditary spastic paraplegia that has material basis in mutation in the KIF5A gene on chromosome 12q13
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Summary
hereditary spastic paraplegia 10 is a rare disease[1].
Key Facts
- hereditary spastic paraplegia 10's instance of is recorded as rare disease[2].
- hereditary spastic paraplegia 10's instance of is recorded as class of disease[3].
- hereditary spastic paraplegia 10 is a type of hereditary spastic paraplegia[4].
- hereditary spastic paraplegia 10 is a type of pure or complex autosomal dominant spastic paraplegia[5].
- hereditary spastic paraplegia 10 is a type of autosomal dominant disease[6].
- hereditary spastic paraplegia 10's NCI Thesaurus ID is recorded as C192058[7].
- hereditary spastic paraplegia 10's health specialty is recorded as neurology[8].
- hereditary spastic paraplegia 10's genetic association is recorded as KIF5A[9].
- hereditary spastic paraplegia 10's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110763[10].
- hereditary spastic paraplegia 10's exact match is recorded as http://identifiers.org/doid/DOID:0110763[11].
- hereditary spastic paraplegia 10's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_100991[12].
- hereditary spastic paraplegia 10's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].