ZFIN Human Disease: hereditary spastic paraplegia 8

OBO ID: DOID:0110823

Term Name:	hereditary spastic paraplegia 8		Search Ontology:
Synonyms:	autosomal dominant spastic paraplegia 8 autosomal dominant spastic paraplegia type 8 SPG8
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the KIAA0196 gene on chromosome 8q24. https://www.ncbi.nlm.nih.gov/pubmed/17160902
References:	GARD:9591 ICD10CM:G11.4 OMIM:603563 ORDO:100989
Ontology:	Human Disease ( DOID:0110823 )

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 8 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
WASHC5	washc5	Spastic paraplegia 8, autosomal dominant	603563

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None