Meckel syndrome, type 3

MONDO:0011821

Any Meckel syndrome in which the cause of the disease is a mutation in the TMEM67 gene.

Also known as: MKS3, Meckel syndrome caused by mutation in TMEM67, Meckel syndrome, type 3, Meckel-Gruber syndrome, type 3, TMEM67 Meckel syndrome, Meckel syndrome 3, Meckel syndrome type 3

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Broader categories

Disease (680) Musculoskeletal system disorder (207) Hereditary disease (176) Bone disorder (51) Syndromic disease (25) Human disease (14) Skeletal system disorder (4) Syndactyly (3) Ciliopathy (2) Disease by molecular mechanism (2)

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