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DO Term : Rothmund-Thomson syndrome [DOID:2732] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A skin disease characterized by poikiloderma, congenital bone defects, and an increased risk of osteosarcoma in childhood and skin cancer later in life that has_material_basis_in homozygous or compound heterozygous mutation in the DNA helicase gene RECQL4 on chromosome 8q24.
  • synonyms:
  • UMLS_CUI:C0032339,
  • SNOMEDCT_US_2023_03_01:205572001,
  • Congenital poikiloderma,
  • MESH:D011038,
  • 268400,
  • OMIM:268400,
  • RTS,
  • ICD10CM:Q82.8,
  • GARD:4392,
  • NCI:C3335
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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