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DO Term : Hajdu-Cheney syndrome [DOID:2736] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A bone disease characterized by short stature, coarse and dysmorphic facies, bowing of the long bones, and vertebral anomalies that has_material_basis_in heterozygous mutation in the NOTCH2 gene on chromosome 1p12.
  • synonyms:
  • DOID:2735,
  • HJCYS,
  • arthrodentoosteodysplasia,
  • 102500,
  • SNOMEDCT_US_2023_03_01:63122002,
  • serpentine fibula-polycystic kidney syndrome,
  • Cheney syndrome,
  • NCI:C84745,
  • NCI:C35545,
  • MESH:D031845,
  • MESH:D030981,
  • OMIM:102500,
  • UMLS_CUI:C0917715,
  • GARD:508,
  • acroosteolysis with osteoporosis and changes in skull and mandible,
  • UMLS_CUI:C0917990,
  • SFPKS
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Disease

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Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents