ZFIN Human Disease: hereditary spastic paraplegia 10

OBO ID: DOID:0110763

Term Name:	hereditary spastic paraplegia 10		Search Ontology:
Synonyms:	autosomal dominant spastic paraplegia 10 autosomal dominant spastic paraplegia type 10 SPG10
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the KIF5A gene on chromosome 12q13. https://www.ncbi.nlm.nih.gov/pubmed/12355402
References:	GARD:9590 ICD10CM:G11.4 OMIM:604187 ORDO:100991
Ontology:	Human Disease ( DOID:0110763 )

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 10 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
KIF5A	kif5aa kif5ab	Spastic paraplegia 10, autosomal dominant	604187

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None