ZFIN Human Disease: hereditary spastic paraplegia 73

OBO ID: DOID:0110818

Term Name:	hereditary spastic paraplegia 73		Search Ontology:
Synonyms:	autosomal dominant spastic paraplegia 73 autosomal dominant spastic paraplegia type 73 SPG73
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
References:	ICD10CM:G11.4 OMIM:616282 ORDO:444099
Ontology:	Human Disease ( DOID:0110818 )

Relationships

is a type of:	autosomal dominant disease hereditary spastic paraplegia autosomal dominant disease hereditary spastic paraplegia Show first 5 Terms

OTHER hereditary spastic paraplegia 73 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CPT1C		?Spastic paraplegia 73, autosomal dominant

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None