Summary Literature (0)

DOID:0110852 - rhizomelic chondrodysplasia punctata type 2

Disease Ontology Definition:A rhizomelic chondrodysplasia punctata that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the GNPAT gene on chromosome 1q42.2.

Synonyms: Chondrodysplasia Punctata, Rhizomelic, Due To Dihydroxyacetonephosphate Acyltransferase Deficiency, Dhapat Deficiency, DHAPAT deficiency, Dihydroxyacetonephosphate Acyltransferase Deficiency, Glyceronephosphate O-Acyltransferase Deficiency, Gnpat Deficiency, GNPAT deficiency, Peroxisomal Dihydroxyacetonephosphate Acyltransferase Deficiency, Rcdp2, RCDP2

Xenbase Genes : gnpat

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0009112 - rhizomelic chondrodysplasia punctata type 2

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee