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 4 ID (Ontology) DOID:0070549 (Human Disease)
Definition A primary pigmented nodular adrenocortical disease that has_material_basis_in duplication on chromosome 19p13 that includes the PRKACA gene.
Also Known As "chromosome 19p13 duplication syndrome" ; "PPNAD4"
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 Genes
 primary pigmented nodular adrenocortical disease 4       3
 for disease ribbon | primary pigmented nodular adrenocortical disease 4       3
 model of | primary pigmented nodular adrenocortical disease 4       3
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autosomal genetic disease
 |__autosomal dominant disease________________________
adrenal cortex disease                                |
 |__primary pigmented nodular adrenocortical disease__|
                                                      primary pigmented nodular adrenocortical disease 4  3 rec.
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Is a autosomal dominant disease
primary pigmented nodular adrenocortical disease
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Synonyms
  • "chromosome 19p13 duplication syndrome" EXACT
    "PPNAD4" EXACT OMO:0003012
Secondary IDs
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MIM:615830