Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1

MONDO:0800436

Any craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development in which the cause of the disease is a variation in the TMCO1 gene.

Also known as: CFSMR1, cerebrofaciothoracic dysplasia, pascual-Castroviejo syndrome type 1, CFSMR, cerebro facio thoracic dysplasia, pascual-Castroviejo syndrome

0 clinical trials for this condition and its sub-types, 0 tagged with Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1 itself.

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