Hypercortisolism

Symptom Information:

Symptom ID: HPO:0001578
Synonyms:
Cushing syndrome [HPO:0001578]
Increased cortisol production [HPO:0001578]
Cushingoid morphotype [Orphanet:53750]
Cushing syndrome [OMIM:Cushing syndrome]
Cushing's syndrome [MedDRA:10011652]
Quality:
Cross references:
Orphanet:53750 "Cushingoid morphotype" [Orphanet:53750]
OMIM: "Cushing syndrome" [OMIM:Cushing syndrome]
UMLS:C0010481 "Hypercortisolism" [HPO:0001578]
Is a (Direct Parents):
MedDRA Endocrine and metabolic secondary hypertension
HPO         Adrenal overactivity
Orphanet Build/stature/longevity anomalies
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)
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)