ZFIN Human Disease: hereditary spastic paraplegia 3A

OBO ID: DOID:0110791

Term Name:	hereditary spastic paraplegia 3A		Search Ontology:
Synonyms:	autosomal dominant familial spastic paraplegia 1 autosomal dominant spastic paraplegia 3 autosomal dominant spastic paraplegia type 3 FSP1 SPG3A strumpell disease
Definition:	A hereditary spastic paraplegia that is characterized by lower limb weakness and spasticity that is generally non-progressive or extremely slow and has_material_basis_in mutation in the ATL1 gene on chromosome 14q22. https://www.ncbi.nlm.nih.gov/pubmed/11685207
References:	GARD:5041 ICD10CM:G11.4 OMIM:182600 ORDO:100984
Ontology:	Human Disease ( DOID:0110791 )

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 3A PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
ATL1	atl1	Spastic paraplegia 3A, autosomal dominant	182600

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None