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DO Term : Mowat-Wilson syndrome [DOID:0060485] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A syndrome characterized by distinctive facial features, intellectual disability, delayed development, Hirschsprung disease and has_material_basis_in de novo heterozygous mutation in the ZEB2 gene on chromosome 2q22.
  • synonyms:
  • GARD:9673,
  • NCI:C74999,
  • MESH:C536990,
  • SNOMEDCT_US_2023_03_01:703535000,
  • OMIM:235730,
  • Hirschsprung disease mental retardation syndrome,
  • ORDO:2152,
  • microcephaly, mental retardation, and distinct facial featrues, with or without Hirschprung disease,
  • 235730,
  • UMLS_CUI:C1856113
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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