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DOID:0070255 - congenital disorder of glycosylation type IIc
Disease Ontology Definition:A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of the SLC35C1 gene on chromosome 11p11.2.
Synonyms: CDG IIc, CDG2C, CDGIIc, Rambam-Hasharon syndrome,
Xenbase Genes : slc35c1
MONDO:0009953 - leukocyte adhesion deficiency type II |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee