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MYH10-related neurodevelopmental disorder with congenital anomalies

MONDO:0700281

An autosomal dominant complex neurodevelopmental disorder in which the cause of the disease is a mutation in the MYH10 gene.

1 clinical trial for this condition and its sub-types, 0 tagged with MYH10-related neurodevelopmental disorder with congenital anomalies itself.

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↑ Autosomal dominant disease (699) ↑ Mendelian neurodevelopmental disorder (208) ↑ Complex neurodevelopmental disorder with or without congenital anomalies (0)
Including sub-types (1) Tagged with MYH10-related neurodevelopmental disorder with congenital anomalies (0)

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