ZFIN Human Disease: hereditary spastic paraplegia 12

OBO ID: DOID:0110765

Term Name:	hereditary spastic paraplegia 12		Search Ontology:
Synonyms:	autosomal dominant spastic paraplegia 12 autosomal dominant spastic paraplegia type 12 SPG12
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the RTN2 gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/22232211
References:	GARD:9586 ICD10CM:G11.4 OMIM:604805 ORDO:100993
Ontology:	Human Disease ( DOID:0110765 )

Relationships

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

OTHER hereditary spastic paraplegia 12 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
RTN2	rtn2b rtn2a	Spastic paraplegia 12, autosomal dominant	604805

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None