ZFIN Human Disease: hereditary spastic paraplegia 62

OBO ID: DOID:0110813

Term Name:	hereditary spastic paraplegia 62		Search Ontology:
Synonyms:	autosomal recessive spastic paraplegia 62 autosomal recessive spastic paraplegia type 62 SPG62
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the ERLIN1 gene on chromosome 10q24. https://www.ncbi.nlm.nih.gov/pubmed/24482476
References:	ICD10CM:G11.4 OMIM:615681 ORDO:401785
Ontology:	Human Disease ( DOID:0110813 )

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 62 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
ERLIN1	erlin1	Spastic paraplegia 62, autosomal recessive	615681

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None