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Summary Literature (0)
MIM:300868 - MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2

Xenbase Genes: piga

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010466 - multiple congenital anomalies-hypotonia-seizures syndrome 2

Disease Ontology (DO):
DOID:0080139 - multiple congenital anomalies-hypotonia-seizures syndrome 2