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Metadata
ID DOID:0110818
Name hereditary spastic paraplegia 73
Definition A hereditary spastic paraplegia that has_material_basis_in mutation in the CPT1C gene on chromosome 19q13.
https://www.ncbi.nlm.nih.gov/pubmed/25751282
Xrefs

ICD10CM:G11.4

OMIM:616282

ORDO:444099

Subsets

DO_rare_slim

Synonyms

autosomal dominant spastic paraplegia 73 [EXACT]

autosomal dominant spastic paraplegia type 73 [EXACT]

SPG73 [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

is_a autosomal dominant disease

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