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congenital disorder of glycosylation Id
Summary
- Synonym
-
- congenital disorder of glycosylation 1d
- Definition
- A congenital disorder of glycosylation I that is characterized by severe neurologic involvement associated with dysmorphism and visual impairment and has_material_basis_in homozygous or compound heterozygous mutation in the ALG3 gene on chromosome 3q27.
- Super Class
- autosomal recessive disease congenital disorder of glycosylation type I
External Links
- Disease Ontology
- DOID:0080556
- Mondo Disease Ontology
- ORDO
- OMIM
- GARD
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| O15305 | Phosphomannomutase 2 | |
| O75352 | Mannose-P-dolichol utilization defect 1 protein |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001332 | Dystonia |
| HP:0001410 | Decreased liver function |
| HP:0001638 | Cardiomyopathy |
| HP:0001871 | Abnormality of blood and blood-forming tissues |
| HP:0002060 | Abnormal cerebral morphology |
| HP:0002079 | Hypoplasia of the corpus callosum |
| HP:0002086 | Abnormality of the respiratory system |
| HP:0002089 | Pulmonary hypoplasia |
| HP:0002719 | Recurrent infections |
| HP:0002804 | Arthrogryposis multiplex congenita |
