ZFIN Human Disease: hereditary spastic paraplegia 75

OBO ID: DOID:0110820

Term Name:	hereditary spastic paraplegia 75		Search Ontology:
Synonyms:	autosomal recessive spastic paraplegia 75 autosomal recessive spastic paraplegia type 75 SPG75
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the MAG gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/24482476
References:	ICD10CM:G11.4 OMIM:616680 ORDO:459056
Ontology:	Human Disease ( DOID:0110820 )

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 75 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
MAG	mag	Spastic paraplegia 75, autosomal recessive	616680

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None