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

0 clinical trials for this condition and its sub-types, 0 tagged with Pitt-Hopkins-like syndrome 2 itself.

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↑ Congenital nervous system disorder (287) ↑ Mendelian neurodevelopmental disorder (208) ↑ Pitt-Hopkins-like syndrome (0)

Including sub-types (0) Tagged with Pitt-Hopkins-like syndrome 2 (0)

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