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Summary Literature (0)
MIM:614080 - MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1; MCAHS1

Xenbase Genes: pign

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013563 - multiple congenital anomalies-hypotonia-seizures syndrome 1

Disease Ontology (DO):
DOID:0080138 - multiple congenital anomalies-hypotonia-seizures syndrome 1