multiple congenital anomalies-hypotonia-seizures syndrome 1 (Q26492831)
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Human disease
- PIGN-CDG
- MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1; MCAHS1
- Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome type 1
- MCAHS1
- MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1
- Multiple congenital anomalies-hypotonia-seizures syndrome
- Congenital disorder of glycosylation due to PIGN deficiency
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | multiple congenital anomalies-hypotonia-seizures syndrome 1 |
Human disease |
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C176896
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