Search Ontology:
Human Disease
primary pigmented nodular adrenocortical disease 2
- Term ID
- DOID:0070547
- Synonyms
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- PPNAD2
- Definition
- A primary pigmented nodular adrenocortical disease that has_material_basis_in heterozygous mutation in the PDE11A gene on chromosome 2q31.2. https://pubmed.ncbi.nlm.nih.gov/16767104/
- References
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- MESH:C566472
- MIM:610475
- UMLS_CUI:C1864851
- Ontology
- Human Disease ( DOID:0070547 )
- is a type of
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