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DO Term : neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures [DOID:0081327] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A neurodegenerative disease that is characterized by neurodevelopmental regression that became apparent between 2 and 10 years of age after normal early development in most patients, although a few had mild early delays and that has_material_basis_in heterozygous mutation in the IRF2BPL gene on chromosome 14q24.
  • synonyms:
  • NEDAMSS,
  • OMIM:618088,
  • 618088
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents