ZFIN Human Disease: hereditary spastic paraplegia 77

OBO ID: DOID:0110822

Term Name:	hereditary spastic paraplegia 77		Search Ontology:
Synonyms:	autosomal recessive spastic paraplegia 77 SPG77
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the FARS2 gene on chromosome 6p25. https://www.ncbi.nlm.nih.gov/pubmed/26553276
References:	ICD10CM:G11.4 OMIM:617046 ORDO:466722
Ontology:	Human Disease ( DOID:0110822 )

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 77 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
FARS2	fars2	Spastic paraplegia 77, autosomal recessive	617046

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None