Any 3-M syndrome in which the cause of the disease is a mutation in the CCDC8 gene.
Comprehensive, easy-to-understand information about this condition
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microcephalic osteodysplastic primordial dwarfism type II
MONDO:0008872
Lowry-Wood syndrome
MONDO:0009191
Hallermann-Streiff syndrome
MONDO:0009318
hypoparathyroidism-retardation-dysmorphism syndrome
MONDO:0009426
microcephalic primordial dwarfism, Toriello type
MONDO:0009616
3M syndrome 1
MONDO:0010117