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DO Term : Saul-Wilson syndrome [DOID:0111673] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A bone development disease characterized by early developmental delay primarily involving speech, distinct facial features, short stature, brachydactyly, clubfoot deformities, cataracts, and microcephaly that has_material_basis_in heterozygous mutation in the COG4 gene on chromosome 16q22.1.
  • synonyms:
  • ORDO:85172,
  • SWILS,
  • OMIM:618150,
  • microcephalic osteodysplastic dysplasia, Saul-Wilson type,
  • 618150,
  • UMLS_CUI:C1300285,
  • SNOMEDCT_US_2023_03_01:389197004
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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