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MIRAGE
congenital disorder of glycosylation Ie
Summary
- Synonym
-
- congenital disorder of glycosylation 1e
- Definition
- A congenital disorder of glycosylation I that is characterized by psychomotor delay, seizures, hypotonia, facial dysmorphism and microcephaly and has_material_basis_in homozygous or compound heterozygous mutation in the DPM1 gene on chromosome 20q13.
- Super Class
- autosomal recessive disease congenital disorder of glycosylation type I
External Links
- Disease Ontology
- DOID:0080557
- Mondo Disease Ontology
- ORDO
- GARD
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001847 | Long hallux |
| HP:0001852 | Sandal gap |
| HP:0001976 | Reduced antithrombin III activity |
| HP:0002014 | Diarrhea |
| HP:0002057 | Prominent glabella |
| HP:0002059 | Cerebral atrophy |
| HP:0002119 | Ventriculomegaly |
| HP:0002123 | Generalized myoclonic seizure |
| HP:0002164 | Nail dysplasia |
| HP:0002240 | Hepatomegaly |
