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DO Term : xeroderma pigmentosum group B [DOID:0110850] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A xeroderma pigmentosum characterized by that has_material_basis_in mutation in the ERCC3 gene on chromosome 2q14.
  • synonyms:
  • XPB,
  • OMIM:610651,
  • XP group B,
  • XPBC,
  • 610651,
  • ICD10CM:Q82.1
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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





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