hereditary spastic paraplegia 73
hereditary spastic paraplegia that has material basis in mutation in the CPT1C gene on chromosome 19q13
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hereditary spastic paraplegia 73
Summary
hereditary spastic paraplegia 73 is a rare disease[1]. It is known by 7 alternative names across languages and contexts.[2]
Key Facts
- hereditary spastic paraplegia 73's instance of is recorded as rare disease[3].
- hereditary spastic paraplegia 73's instance of is recorded as class of disease[4].
- hereditary spastic paraplegia 73 is a type of hereditary spastic paraplegia[5].
- hereditary spastic paraplegia 73 is a type of autosomal dominant pure spastic paraplegia[6].
- hereditary spastic paraplegia 73 is a type of autosomal dominant disease[7].
- hereditary spastic paraplegia 73's health specialty is recorded as neurology[8].
- hereditary spastic paraplegia 73's genetic association is recorded as CPT1C[9].
- hereditary spastic paraplegia 73's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110818[10].
- hereditary spastic paraplegia 73's exact match is recorded as http://identifiers.org/doid/DOID:0110818[11].
- hereditary spastic paraplegia 73's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_444099[12].
- hereditary spastic paraplegia 73's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
Why It Matters
hereditary spastic paraplegia 73 is known by 7 alternative names across languages and contexts.[2]