ZFIN Human Disease: hereditary spastic paraplegia 7

OBO ID: DOID:0110816

Term Name:	hereditary spastic paraplegia 7		Search Ontology:
Synonyms:	autosomal recessive spastic paraplegia 7 spastic paraplegia type 7 SPG7
Definition:	A hereditary spastic paraplegia that is characterized by slowly progressive onset, usually between 18-60 years of age, and generally more severe spasticity and has_material_basis_in mutation in the SPG7 gene on chromosome 16q24. https://www.ncbi.nlm.nih.gov/pubmed/9635427
References:	ICD10CM:G11.4 OMIM:607259 ORDO:99013
Ontology:	Human Disease ( DOID:0110816 )

Relationships

is a type of:	autosomal recessive disease hereditary spastic paraplegia autosomal recessive disease hereditary spastic paraplegia Show first 5 Terms

OTHER hereditary spastic paraplegia 7 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SPG7	spg7	Spastic paraplegia 7, autosomal recessive	607259

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None