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MIRAGE
congenital disorder of glycosylation type IIl
Summary
- Synonym
-
- CDG IIl
- CDG syndrome type IIL
- CDG2L
- CDGIIl
- 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
- 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:0000966 | Hypohidrosis |
| HP:0001249 | Intellectual disability |
| HP:0001250 | Seizure |
| HP:0001263 | Global developmental delay |
| HP:0001272 | Cerebellar atrophy |
| HP:0001290 | Generalized hypotonia |
| HP:0001385 | Hip dysplasia |
| HP:0001394 | Cirrhosis |
| HP:0001396 | Cholestasis |
| HP:0001508 | Failure to thrive |
