ZFIN Human Disease: hereditary spastic paraplegia 31

OBO ID: DOID:0110782

Term Name:	hereditary spastic paraplegia 31		Search Ontology:
Synonyms:	autosomal dominant spastic paraplegia 31 autosomal dominant spastic paraplegia type 31 SPG31
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the REEP1 gene on chromosome 2p11. https://www.ncbi.nlm.nih.gov/pubmed/16826527
References:	GARD:10817 ICD10CM:G11.4 OMIM:610250 ORDO:101011
Ontology:	Human Disease ( DOID:0110782 )

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 31 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
REEP1	reep1	Spastic paraplegia 31, autosomal dominant	610250

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None