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ARHGAP29-related non-syndromic orofacial cleft

MONDO:1060132

Any orofacial cleft in which the cause of the disease is a mutation in the ARHGAP29 gene.

1 clinical trial for this condition and its sub-types.

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Broader categories

Disease (680) Musculoskeletal system disorder (207) Hereditary disease (176) Bone disorder (51) Human disease (14) Disorder of facial skeleton (4) Orofacial cleft (4) Skeletal system disorder (4) Disease of genetic or genomic mechanism (2) Skull disorder (1)
Completed 1
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