Pigmented micronodular adrenocortical disease

Symptom Information:

Symptom ID: HPO:0001580
Synonyms:
Pigmented micronodular adrenocortical disease [OMIM:Pigmented micronodular adrenocortical disease]
Quality:
Cross references:
OMIM: "Pigmented micronodular adrenocortical disease" [OMIM:Pigmented micronodular adrenocortical disease]
Is a (Direct Parents):
HPO         Adrenocortical abnormality
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the endocrine system(HPO:0000818)
          Abnormality of the adrenal glands(HPO:0000834)
             Abnormality of adrenal morphology(HPO:0011732)
                Adrenocortical abnormality(HPO:0000849)
                   Pigmented micronodular adrenocortical disease(HPO:0001580)
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Carney complex (Orphanet:1359)
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1 (OMIM:610489)
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2 (OMIM:610475)
Primary pigmented nodular adrenocortical disease (Orphanet:189439)