3M syndrome 3

MONDO:0013627

Any 3-M syndrome in which the cause of the disease is a mutation in the CCDC8 gene.

Also known as: 3-M syndrome 3, 3-M syndrome caused by mutation in CCDC8, 3M syndrome 3, CCDC8 3-M syndrome, three M syndrome 3, three M syndrome type 3, 3M3

0 clinical trials for this condition and its sub-types, 0 tagged with 3M syndrome 3 itself.

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Part of

↑ Primordial dwarfism and slender bone disorder (9) ↑ 3-M syndrome (0)

Including sub-types (0) Tagged with 3M syndrome 3 (0)

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