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Neurocristopathy, CHD7-related, cattle

MONDO:1012577

Any neurocristopathy in cattle in which the cause of the disease is a mutation in the CHD7 gene.

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

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Broader categories

Disease (618) Disorder of development or morphogenesis, non-human animal (0) Hereditary disease, non-human animal (0) Neurocristopathy, non-human animal (0) Non-human animal disease (0)

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