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congenital disorder of glycosylation type IIl
Summary
- Synonym
-
- CDG IIl
- CDG syndrome type IIL
- CDG2L
- CDGIIdl
- COG6-CGD
- Congenital disorder of glycosylation type 2l
- Definition
- A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of the COG6 gene on chromosome 13q14.11.
- Super Class
- autosomal recessive disease congenital disorder of glycosylation type II
External Links
- Disease Ontology
- DOID:0070264
- Mondo Disease Ontology
- ORDO
- OMIM
- GARD
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q9Y2V7 | Conserved oligomeric Golgi complex subunit 6 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002028 | Chronic diarrhea |
| HP:0002037 | Inflammation of the large intestine |
| HP:0002040 | Esophageal varix |
| HP:0002059 | Cerebral atrophy |
| HP:0002079 | Hypoplasia of the corpus callosum |
| HP:0002119 | Ventriculomegaly |
| HP:0002240 | Hepatomegaly |
| HP:0002536 | Abnormal cortical gyration |
| HP:0002719 | Recurrent infections |
| HP:0002848 | Decreased specific anti-polysaccharide antibody level |
