FAM111A-related skeletal dysplasia

MONDO:1060172

Any skeletal dysplasia in which the cause of the disease is a variation in FAM111A gene.

Also known as: FAM111A-related skeletal dysplasia

0 clinical trials for this condition and its sub-types, 0 tagged with FAM111A-related skeletal dysplasia itself.

Where it sits in the disease tree

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Sub-types of FAM111A-related skeletal dysplasia

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