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DO Term : Bowen-Conradi syndrome [DOID:0050684] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A syndrome that is characterized by growth delays, failure to thrive and malformations of the head and face that results in infantile death, has_material_basis_in homozygous mutation in the EMG1 gene on chromosome 12p13.
  • synonyms:
  • SNOMEDCT_US_2023_03_01:711153001,
  • BWCNS,
  • OMIM:211180,
  • MESH:C537081,
  • 211180,
  • Bowen Hutterite syndrome,
  • UMLS_CUI:C1859405,
  • ORDO:1270,
  • Bowen-Conradi Hutterite syndrome,
  • GARD:5950
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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