ZFIN Human Disease: hereditary spastic paraplegia 4

OBO ID: DOID:0110792

Term Name:	hereditary spastic paraplegia 4		Search Ontology:
Synonyms:	autosomal dominant spastic paraplegia 4 autosomal dominant spastic paraplegia type 4 SPG4
Definition:	A hereditary spastic paraplegia that is characterized by slowly progressive muscle weakness and spasticity and has_material_basis_in mutation in the SPAST gene on chromosome 2p22. https://www.ncbi.nlm.nih.gov/pubmed/9302257
References:	ICD10CM:G11.4 OMIM:182601 ORDO:100985
Ontology:	Human Disease ( DOID:0110792 )

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 4 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SPAST	spast	Spastic paraplegia 4, autosomal dominant	182601

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None