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Summary Literature (0)
MIM:618088 - NEURODEVELOPMENTAL DISORDER WITH REGRESSION, ABNORMAL MOVEMENTS, LOSS OF SPEECH, AND SEIZURES; NEDAMSS

Xenbase Genes: irf2bpl

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0060759 - neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures

Disease Ontology (DO):
DOID:0081327 - neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures