(Q26492832)
English
multiple congenital anomalies-hypotonia-seizures syndrome 2
Human disease
- MCAHS2
- MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2
- MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2
- Epileptic Encephalopathy, Early Infantile, 20
- MCAHS type 2
- Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome type 2
- glycosylphosphatidylinositol biosynthesis defect 4
- early infantile epileptic encephalopathy 20
- obsolete multiple congenital anomalies-hypotonia-seizures syndrome 2
Statements
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
3 references
1 reference
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference