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MIRAGE
multiple congenital anomalies-hypotonia-seizures syndrome 2
Summary
- Synonym
-
- developmental and epileptic encephalopathy 20
- early infantile epileptic encephalopathy 20
- glycosylphosphatidylinositol biosynthesis defect 4
- Definition
- A multiple congenital anomalies-hypotonia-seizures syndrome that is characterized by X-linked recessive inheritance of dysmorphic features, neonatal hypotonia, myoclonic seizures and variable abnormalities involving the central nervous, cardiac, and urinary systems that has_material_basis_in mutation in the PIGA gene on chromosome Xp22.
- Super Class
- X-linked recessive disease multiple congenital anomalies-hypotonia-seizures syndrome
External Links
- Disease Ontology
- DOID:0080139
- Mondo Disease Ontology
- ORDO
- GARD
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P37287 | Phosphatidylinositol N-acetylglucosaminyltransferase subunit A |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001331 | Absent septum pellucidum |
| HP:0001341 | Olfactory lobe agenesis |
| HP:0001344 | Absent speech |
| HP:0001347 | Hyperreflexia |
| HP:0001348 | Brisk reflexes |
| HP:0001371 | Flexion contracture |
| HP:0001394 | Cirrhosis |
| HP:0001414 | Microvesicular hepatic steatosis |
| HP:0001419 | X-linked recessive inheritance |
| HP:0001520 | Large for gestational age |
