Multiple congenital anomalies, hypotonia, seizures syndrome type 2 (disorder)
| Code | 773643006 |
|---|---|
| Semantic tag | disorder |
| Module | international |
| Definition | primitive |
| Effective time | 20190131 |
238049009Carbohydrate-deficient glycoprotein syndrome
disorder
1275631007Developmental and epileptic encephalopathy
disorder
363070008Developmental hereditary disorder
disorder
128190004Inherited metabolic disorder of nervous system
disorder
65094009Multiple malformation syndrome with facial defects as major feature
disorder
1162976004X-linked recessive hereditary disease
disorder
None (leaf concept).