ZFIN Human Disease: hereditary spastic paraplegia 72A

OBO ID: DOID:0110817

Term Name:	hereditary spastic paraplegia 72A		Search Ontology:
Synonyms:	autosomal spastic paraplegia type 72 SPG72
Definition:	A hereditary spastic paraplegia that has_material_basis_in a heterozygous mutation in the REEP2 gene on chromosome 5q31.2. https://www.ncbi.nlm.nih.gov/pubmed/24388663
References:	ICD10CM:G11.4 OMIM:615625 ORDO:401849
Ontology:	Human Disease ( DOID:0110817 )

Relationships

is a type of:	autosomal dominant disease autosomal recessive disease hereditary spastic paraplegia autosomal dominant disease autosomal recessive disease hereditary spastic paraplegia Show first 5 Terms

OTHER hereditary spastic paraplegia 72A PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
REEP2	reep2	Spastic paraplegia 72A, autosomal dominant	615625

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None