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DO Term : primary pigmented nodular adrenocortical disease 2 [DOID:0070547] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A primary pigmented nodular adrenocortical disease that has_material_basis_in heterozygous mutation in the PDE11A gene on chromosome 2q31.2.
  • synonyms:
  • MESH:C566472,
  • UMLS_CUI:C1864851,
  • PPNAD2,
  • OMIM:610475,
  • 610475
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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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