FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term primary pigmented nodular adrenocortical disease 2 ID (Ontology) DOID:0070547 (Human Disease)
Definition A primary pigmented nodular adrenocortical disease that has_material_basis_in heterozygous mutation in the PDE11A gene on chromosome 2q31.2.
Also Known As "PPNAD2"
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 Genes
 primary pigmented nodular adrenocortical disease 2       1
 for disease ribbon | primary pigmented nodular adrenocortical disease 2       1
 model of | primary pigmented nodular adrenocortical disease 2       1
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autosomal genetic disease
 |__autosomal dominant disease________________________
adrenal cortex disease                                |
 |__primary pigmented nodular adrenocortical disease__|
                                                      primary pigmented nodular adrenocortical disease 2  1 rec.
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Is a autosomal dominant disease
primary pigmented nodular adrenocortical disease
Part of
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Synonyms
  • "PPNAD2" EXACT OMO:0003012
Secondary IDs
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MESH:C566472
MIM:610475
UMLS_CUI:C1864851