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Summary Literature (0)
MIM:615398 - MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3

Xenbase Genes: pigt

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014165 - multiple congenital anomalies-hypotonia-seizures syndrome 3

Disease Ontology (DO):
DOID:0080140 - multiple congenital anomalies-hypotonia-seizures syndrome 3