ZFIN Human Disease: hereditary spastic paraplegia 64

OBO ID: DOID:0110815

Term Name:	hereditary spastic paraplegia 64		Search Ontology:
Synonyms:	autosomal recessive spastic paraplegia 64 autosomal recessive spastic paraplegia type 64 SPG64
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the ENTPD1 gene on chromosome 10q24. https://www.ncbi.nlm.nih.gov/pubmed/24482476
References:	ICD10CM:G11.4 OMIM:615683 ORDO:401810
Ontology:	Human Disease ( DOID:0110815 )

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 64 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
ENTPD1	entpd1	Spastic paraplegia 64, autosomal recessive	615683

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None