Pitt-Hopkins-like syndrome 2

MONDO:0013690

Any Pitt-Hopkins-like syndrome in which the cause of the disease is a mutation in the NRXN1 gene.

Also known as: NRXN1 Pitt-Hopkins-like syndrome, NRXN1-related severe neurodevelopmental disorder-motor stereotypies-chronic constipation-sleep-wake cycle disturbance, PTHSL2, Pitt-Hopkins-like syndrome 2, Pitt-Hopkins-like syndrome caused by mutation in NRXN1, Pitt-Hopkins-like syndrome type 2

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

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