ZFIN Human Disease: hereditary spastic paraplegia 76

OBO ID: DOID:0110821

Term Name:	hereditary spastic paraplegia 76		Search Ontology:
Synonyms:	autosomal recessive spastic paraplegia 76 SPG76
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the CAPN1 gene on chromosome 11q13. https://www.ncbi.nlm.nih.gov/pubmed/27153400
References:	OMIM:616907
Ontology:	Human Disease ( DOID:0110821 )

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 76 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CAPN1	capn1b capn1a capn1	Spastic paraplegia 76, autosomal recessive	616907

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None