ZFIN Human Disease: hereditary spastic paraplegia 46

OBO ID: DOID:0110798

Term Name:	hereditary spastic paraplegia 46		Search Ontology:
Synonyms:	autosomal recessive spastic paraplegia 46 autosomal recessive spastic paraplegia type 46 SPG46
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the GBA2 gene on chromosome 9p. https://www.ncbi.nlm.nih.gov/pubmed/23332916
References:	ICD10CM:G11.4 OMIM:614409 ORDO:320391
Ontology:	Human Disease ( DOID:0110798 )

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 46 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
GBA2	gba2	Spastic paraplegia 46, autosomal recessive	614409

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None