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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:0001028 | Hemangioma |
| HP:0001103 | Abnormal macular morphology |
| HP:0001252 | Hypotonia |
| HP:0001290 | Generalized hypotonia |
| HP:0001337 | Tremor |
| HP:0001643 | Patent ductus arteriosus |
| HP:0001744 | Splenomegaly |
| HP:0002098 | Respiratory distress |
| HP:0002353 | EEG abnormality |
| HP:0002395 | Lower limb hyperreflexia |
