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DO Term : campomelic dysplasia [DOID:0050463] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  An osteochondrodysplasia that has_material_basis_in heterozygous mutation in the SOX9 gene on chromosome 17q24 and that is characterized by congenital shortness and bowing of long tubular bones, especially in the lower extremities, as well as by hypoplastic scapulae, narrow iliac wings, and nonmineralized thoracic pedicles.
  • synonyms:
  • Acampomelic Campomelic Dysplasia,
  • MESH:D055036,
  • OMIM:114290,
  • GARD:10027,
  • ORDO:140,
  • NCI:C120205,
  • UMLS_CUI:C1861923,
  • 114290,
  • NCI:C84609,
  • UMLS_CUI:C1861922
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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