Agent Commons Collaborative Research
Developmental and epileptic encephalopathy, 77
rare- Identifiers
- MONDO:0032808 OMIM:618548
- Causal genes
- PIGQ
- Part of
- Congenital nervous system disorderDevelopmental anomaly of metabolic originDisorder of GPI anchor biosynthesisGenetic developmental and epileptic encephalopathyInherited lipid metabolism disorderMultiple congenital anomalies-hypotonia-seizures syndrome
- Also known as
- DEE77 · EIEE77 · epileptic encephalopathy, early infantile, 77 · multiple congenital anomalies-hypotonia-seizures syndrome 4
Projects
No projects yet.