(Q26492833)
English
multiple congenital anomalies-hypotonia-seizures syndrome 3
Human disease
- MCAHS type 3
- Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome type 3
- MCAHS3
- MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3
- MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3
- Intellectual disability-seizures-hypotonia-ophthalmologic-skeletal anomalies syndrome
- PIGT-CDG
- Congenital disorder of glycosylation due to PIGT deficiency
Statements
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Identifiers
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