Hypercortisolism
Symptom Information:
Symptom ID: | HPO:0001578 | ||||||
Synonyms: |
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Quality: | |||||||
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 physiology(HPO:0011733) Adrenal overactivity(HPO:0002717) Hypercortisolism(HPO:0001578) MedDRA: Vascular disorders(MedDRA:10047065) Vascular hypertensive disorders(MedDRA:10057166) Endocrine and metabolic secondary hypertension(MedDRA:10052741) Hypercortisolism(HPO:0001578) |
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Database Frequency: | 17 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
ACTH-independent Cushing syndrome | (Orphanet:99893) |
ACTH-independent macronodular adrenal hyperplasia | (Orphanet:189427) |
Bangstad syndrome | (Orphanet:1227) |
Carney complex | (Orphanet:1359) |
Combined oxidative phosphorylation defect type 15 | (Orphanet:319524) |
Cushing disease | (Orphanet:96253) |
Cushing syndrome | (Orphanet:553) |
Fibrous dysplasia of bone | (Orphanet:249) |
McCune-Albright syndrome | (Orphanet:562) |
Multiple endocrine neoplasia type 1 | (Orphanet:652) |
Multiple endocrine neoplasia type 2A | (Orphanet:247698) |
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1 | (OMIM:610489) |
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2 | (OMIM:610475) |
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 3 | (OMIM:614190) |
Polyostotic fibrous dysplasia | (Orphanet:93276) |
Pseudoleprechaunism syndrome, Patterson type | (Orphanet:2976) |
Thymoma | (Orphanet:99867) |