ZFIN Human Disease: hereditary spastic paraplegia 55

OBO ID: DOID:0110807

Term Name:	hereditary spastic paraplegia 55		Search Ontology:
Synonyms:	autosomal recessive spastic paraplegia 55 autosomal recessive spastic paraplegia type 55 SPG55
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the C12ORF65 gene on chromosome 12q24. https://www.ncbi.nlm.nih.gov/pubmed/23188110
References:	ICD10CM:G11.4 OMIM:615035 ORDO:320375
Ontology:	Human Disease ( DOID:0110807 )

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 55 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
C12orf65	mtrfr	Spastic paraplegia 55, autosomal recessive	615035

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None