(Q26492831)
English
multiple congenital anomalies-hypotonia-seizures syndrome 1
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
Statements
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C176896
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Identifiers
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