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 is a type of hereditary spastic paraplegia[4].
- hereditary spastic paraplegia 13 is a type of pure or complex autosomal dominant spastic paraplegia[5].
- hereditary spastic paraplegia 13 is a type of autosomal dominant disease[6].
- hereditary spastic paraplegia 13's health specialty is recorded as neurology[7].
- hereditary spastic paraplegia 13's genetic association is recorded as HSPD1[8].
- hereditary spastic paraplegia 13's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110766[9].
- hereditary spastic paraplegia 13's exact match is recorded as http://identifiers.org/doid/DOID:0110766[10].
- hereditary spastic paraplegia 13's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_100994[11].
- hereditary spastic paraplegia 13's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].