ZFIN Human Disease: hereditary spastic paraplegia 13

OBO ID: DOID:0110766

Term Name:	hereditary spastic paraplegia 13		Search Ontology:
Synonyms:	autosomal dominant spastic paraplegia 13 SPG13
Definition:	A hereditary spastic paraplegia that is characterized by a pure form of the disease with late onset and has_material_basis_in mutation in the HSPD1 gene on chromosome 2q33. https://www.ncbi.nlm.nih.gov/pubmed/11898127
References:	GARD:9616 ICD10CM:G11.4 OMIM:605280 ORDO:100994
Ontology:	Human Disease ( DOID:0110766 )

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 13 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
HSPD1	hspd1	Spastic paraplegia 13, autosomal dominant	605280

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None