ZFIN Human Disease: hereditary spastic paraplegia 56

OBO ID: DOID:0110808

Term Name:	hereditary spastic paraplegia 56		Search Ontology:
Synonyms:	autosomal recessive spastic paraplegia 56 autosomal recessive spastic paraplegia type 56 SPG56
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the CYP2U1 gene on chromosome 4q25. https://www.ncbi.nlm.nih.gov/pubmed/23176821
References:	ICD10CM:G11.4 OMIM:615030 ORDO:320411
Ontology:	Human Disease ( DOID:0110808 )

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 56 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CYP2U1	cyp2u1	Spastic paraplegia 56, autosomal recessive	615030

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None