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MIRAGE
congenital disorder of glycosylation type IIh
Summary
- Synonym
-
- CDG IIh
- CDG2H
- CDGIIh
- COG8-CDG
- Carbohydrate deficient glycoprotein syndrome type IIh
- Congenital disorder of glycosylation type 2h
- Definition
- A congenital disorder of glycosylation type II that has_material_basis_in a mutation of the COG8 gene on chromosome 16q22.1.
- Super Class
- autosomal recessive disease congenital disorder of glycosylation type II
External Links
- Disease Ontology
- DOID:0070260
- Mondo Disease Ontology
- MeSH
- UMLS
- ORDO
- GARD
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q96MW5 | Conserved oligomeric Golgi complex subunit 8 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000253 | Progressive microcephaly |
| HP:0001137 | Alternating esotropia |
| HP:0001249 | Intellectual disability |
| HP:0001250 | Seizure |
| HP:0001251 | Ataxia |
| HP:0001272 | Cerebellar atrophy |
| HP:0001336 | Myoclonus |
| HP:0001508 | Failure to thrive |
| HP:0001943 | Hypoglycemia |
| HP:0002119 | Ventriculomegaly |
