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| Term | primary pigmented nodular adrenocortical disease 1 | ID (Ontology) | DOID:0070546 (Human Disease) |
| Definition | A primary pigmented nodular adrenocortical disease that has_material_basis_in heterozygous mutation in the PRKAR1A gene on chromosome 17q24.2. | ||
| Also Known As | "PPNAD1" | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal genetic disease |__autosomal dominant disease________________________ adrenal cortex disease | |__primary pigmented nodular adrenocortical disease__| primary pigmented nodular adrenocortical disease 1 1 rec. |
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| Is a |
autosomal dominant disease primary pigmented nodular adrenocortical disease |
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External Crossreferences & Linkouts
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MESH:C566469 MIM:610489 UMLS_CUI:C1864846 |
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