Adrenal hyperplasia

Symptom Information:

Symptom ID: HPO:0008221
Synonyms:
Enlarged adrenal glands [HPO:0008221]
Adrenocortical hyperplasia [Orphanet:41450]
Hypercortisolism (disorder) [Orphanet:41450]
Adrenocortical hyperfunction (disorder) [Orphanet:41450]
Adrenal hyperplasia [OMIM:Adrenal hyperplasia]
Enlarged adrenal glands [OMIM:Enlarged adrenal glands]
Cortico-adrenal hyperplasia/hypersecretion [Orphanet:41450]
Hypercorticoidism [Orphanet:41450]
Hyperadrenocorticism [Orphanet:41450]
Hyperadrenalism [Orphanet:41450]
Hypercorticoidism [MedDRA:10020610]
Hypercortisolism [MedDRA:10020610]
Hypercortisonism [MedDRA:10020610]
Hyperadrenocorticism [MedDRA:10020564]
Adrenal cortex activity increased [MedDRA:10020564]
Adrenal cortex hyperfunction [MedDRA:10020564]
Adrenal cortex hyperplasia [MedDRA:10020564]
Adrenal hypercorticism [MedDRA:10020564]
Hyperadrenalcorticalism [MedDRA:10020564]
Hyperadrenocorticalism [MedDRA:10020564]
Hypercorticism adrenal [MedDRA:10020564]
Hyperplasia adrenal cortex [MedDRA:10020564]
Hyperadrenalism [MedDRA:10020562]
Hyperplasia adrenal [MedDRA:10020562]
Other corticoadrenal overactivity [MedDRA:10020562]
Hyperadrenocorticism [OMIM:Hyperadrenocorticism]
Quality:
Cross references:
Orphanet:41450 "Cortico-adrenal hyperplasia/hypersecretion" [Orphanet:41450]
OMIM: "Adrenal hyperplasia" [OMIM:Adrenal hyperplasia]
OMIM: "Enlarged adrenal glands" [OMIM:Enlarged adrenal glands]
OMIM: "Hyperadrenocorticism" [OMIM:Hyperadrenocorticism]
Is a (Direct Parents):
MedDRA Metabolic disorders NEC
HPO         Abnormality of adrenal morphology
Orphanet Abnormality of the adrenal glands
MedDRA Endocrine and metabolic secondary hypertension
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)
                Adrenal hyperplasia(HPO:0008221)
MedDRA:
Metabolism and nutrition disorders(MedDRA:10027433)
    Metabolism disorders NEC(MedDRA:10000546)
       Metabolic disorders NEC(MedDRA:10027428)
          Adrenal hyperplasia(HPO:0008221)
Vascular disorders(MedDRA:10047065)
    Vascular hypertensive disorders(MedDRA:10057166)
       Endocrine and metabolic secondary hypertension(MedDRA:10052741)
          Adrenal hyperplasia(HPO:0008221)
Database Frequency: 24 / 7739
Resource:

All diseases associated with this symptom:

ACTH-independent Cushing syndrome (Orphanet:99893)
ACTH-independent macronodular adrenal hyperplasia (Orphanet:189427)
Autoimmune polyendocrinopathy type 1 (Orphanet:3453)
Bangstad syndrome (Orphanet:1227)
Carney complex (Orphanet:1359)
Carney triad (Orphanet:139411)
Catecholamine-producing tumor (Orphanet:717)
Congenital adrenal hyperplasia (Orphanet:418)
Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency (Orphanet:90795)
Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency (Orphanet:90793)
Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency (Orphanet:90791)
Cushing disease (Orphanet:96253)
Cushing syndrome (Orphanet:553)
Ehlers-Danlos syndrome due to tenascin-X deficiency (Orphanet:230839)
Familial hyperaldosteronism type 1 (Orphanet:403)
Familial hyperaldosteronism type 3 (Orphanet:251274)
McCune-Albright syndrome (Orphanet:562)
Multiple endocrine neoplasia type 1 (Orphanet:652)
Multiple endocrine neoplasia type 2 (Orphanet:653)
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 3 (OMIM:614190)
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4 (OMIM:615830)
Primary pigmented nodular adrenocortical disease (Orphanet:189439)
Pseudoleprechaunism syndrome, Patterson type (Orphanet:2976)
Rabson-Mendenhall syndrome (Orphanet:769)