Pigmented micronodular adrenocortical disease
Symptom Information:
Symptom ID: | HPO:0001580 | ||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |