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3M syndrome 3

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Any 3-M syndrome in which the cause of the disease is a mutation in the CCDC8 gene.
Uniprot Description A disorder characterized by poor postnatal growth and distinctive facial features, including triangular facies, frontal bossing, fleshy tipped nose, and fleshy lips. Other features may include skeletal anomalies and prominent heels.
Mondo Term and Equivalent IDs
MONDO:0013627:  3M syndrome 3
UMLS:C3280146: