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MIM:300868 - MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2
Echinobase Genes:
Human Disease Resource: OMIM
DOID:0080139 - multiple congenital anomalies-hypotonia-seizures syndrome 2 |
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DOID:0080139 - multiple congenital anomalies-hypotonia-seizures syndrome 2 |