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Familial schizencephaly

MONDO:0018829

An instance of schizencephaly that is caused by an inherited modification of the individual's genome.

Also known as: familial schizencephaly, hereditary schizencephaly

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

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Broader categories

Disease (717) Nervous system disorder (243) Hereditary disease (188) Brain disorder (131) Central nervous system disorder (115) Human disease (15) Hereditary neurological disease (6) COL4A1/A2-related disorder (2) Disease of genetic or genomic mechanism (2) COL4A1-related disorder (1)

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