ZFIN Human Disease: hereditary spastic paraplegia 61

OBO ID: DOID:0110812

Term Name:	hereditary spastic paraplegia 61		Search Ontology:
Synonyms:	autosomal recessive spastic paraplegia 61 autosomal recessive spastic paraplegia type 61 SPG61
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the ARL6IP1 gene on chromosome 16p12. https://www.ncbi.nlm.nih.gov/pubmed/24482476
References:	ICD10CM:G11.4 OMIM:615685 ORDO:401780
Ontology:	Human Disease ( DOID:0110812 )

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 61 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
ARL6IP1	arl6ip1	Spastic paraplegia 61, autosomal recessive	615685

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None