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Seckel syndrome 6

MONDO:0013871

Any Seckel syndrome in which the cause of the disease is a mutation in the CEP63 gene.

Also known as: CEP63 Seckel syndrome, SCKL6, Seckel syndrome 6, Seckel syndrome caused by mutation in CEP63, Seckel syndrome type 6

0 clinical trials for this condition and its sub-types.

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Broader categories

Disease (679) Hereditary disease (176) Syndromic disease (25) Human disease (14) Autosomal recessive disease (4) Disease of genetic or genomic mechanism (2) Autosomal genetic disease (0) Disease by body system or component (0) Disease by etiologic mechanism (0) Seckel syndrome (0)

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