Term Name: congenital disorder of glycosylation type IIc
Synonyms: CDG IIc, CDG2C, CDGIIc, Rambam-Hasharon syndrome
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.
Ontology: Human Disease [DOID:0070255]   ( DOID:0070255 )

Relationships
is a type of: autosomal recessive disease congenital disorder of glycosylation type II