ZFIN Human Disease: hereditary spastic paraplegia 53

OBO ID: DOID:0110805

Term Name:	hereditary spastic paraplegia 53		Search Ontology:
Synonyms:	autosomal recessive spastic paraplegia 53 autosomal recessive spastic paraplegia type 53 SPG53
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the VPS37A gene on chromosome 8p22. https://www.ncbi.nlm.nih.gov/pubmed/22717650
References:	ICD10CM:G11.4 OMIM:614898 ORDO:319199
Ontology:	Human Disease ( DOID:0110805 )

Relationships

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

OTHER hereditary spastic paraplegia 53 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
VPS37A	vps37a	Spastic paraplegia 53, autosomal recessive	614898

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None