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Up to: Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome
Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1
Any craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development in which the cause of the disease is a variation in the TMCO1 gene.
This condition has no sub-types.