ZFIN Human Disease: hereditary spastic paraplegia 57

OBO ID: DOID:0110809

Term Name:	hereditary spastic paraplegia 57		Search Ontology:
Synonyms:	autosomal recessive spastic paraplegia 57 autosomal recessive spastic paraplegia type 57 SPG57
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the TFG gene on chromosome 3q12. https://www.ncbi.nlm.nih.gov/pubmed/23479643
References:	ICD10CM:G11.4 OMIM:615658 ORDO:431329
Ontology:	Human Disease ( DOID:0110809 )

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 57 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
TFG	tfg	?Spastic paraplegia 57, autosomal recessive	615658

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None