Schizophrenia 16

MONDO:0013506

A schizophrenia that has material basis in a mutation on chromosome 7q36.3.

Also known as: SCZD16, schizophrenia 16, schizophrenia type 16, chromosome 7Q36.3 Duplication syndrome, 362-Kb, schizophrenia susceptibility locus, chromosome 7Q36.3-related

82 clinical trials for this condition and its sub-types, 0 tagged with Schizophrenia 16 itself.

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Part of

↑ Hereditary neurological disease (5772) ↑ Schizophrenia (651) ↑ Myopia (273)

Including sub-types (82) Tagged with Schizophrenia 16 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.