Mowat-Wilson syndrome due to monosomy 2q22

MONDO:0016855

Also known as: Hirschsprung disease and intellectual disability due to 2q22 microdeletion, Hirschsprung disease and intellectual disability due to del(2)(q22), Hirschsprung disease and intellectual disability due to monosomy 2q22, Mowat-Wilson syndrome due to 2q22 microdeletion, Mowat-Wilson syndrome due to del(2)q(22), Mowat-Wilson syndrome due to monosomy type 2q22

7 clinical trials for this condition and its sub-types, 0 tagged with Mowat-Wilson syndrome due to monosomy 2q22 itself.

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Part of

↑ Mowat-Wilson syndrome (2) ↑ Partial deletion of the long arm of chromosome 2 (2)

Including sub-types (7) Tagged with Mowat-Wilson syndrome due to monosomy 2q22 (0)

Trials to join now! 4 Not yet finished but already full! 2 Completed 1

Routine EEGs may hold hidden clues to childhood epilepsy — a new analysis method is put to the test

Diagnosis Completed

This study is testing whether a computer tool called BioEP can detect signs of seizure susceptibility in standard EEG recordings from children with epilepsy. Researchers will analyze past EEGs from 530 children aged 2 to 18 who already have an epilepsy diagnosis. The goal is to s…

Sponsor: Neuronostics Ltd • Aim: Diagnosis

Last updated Aug 01, 2026 00:00 UTC

Mowat-Wilson syndrome due to monosomy 2q22

Where it sits in the disease tree

Routine EEGs may hold hidden clues to childhood epilepsy — a new analysis method is put to the test