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MIRAGE
congenital disorder of glycosylation type IIa
Summary
- Synonym
-
- Alkuraya syndrome
- CDG IIa
- CDG2A
- CDGIIa
- CDGS2
- carbohydrate-deficient glycoprotein syndrome, type II
- congenital disorder of glycosylation, type IIa
- mental retardation, growth retardation, prominent columella, and open mouth
- Definition
- A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of the MGAT2 gene on chromosome 14q21.3.
- Super Class
- autosomal recessive disease congenital disorder of glycosylation type II
External Links
- Disease Ontology
- DOID:0070253
- Mondo Disease Ontology
- MeSH
- UMLS
- ORDO
- GARD
- MGI genotype (from TogoID)
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q10469 | Alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase |
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q921V5 | Alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000248 | Brachycephaly |
| HP:0000252 | Microcephaly |
| HP:0000256 | Macrocephaly |
| HP:0000278 | Retrognathia |
| HP:0000303 | Mandibular prognathia |
| HP:0000343 | Long philtrum |
| HP:0000369 | Low-set ears |
| HP:0000400 | Macrotia |
| HP:0000407 | Sensorineural hearing impairment |
| HP:0000426 | Prominent nasal bridge |
