Adrenal hyperplasia
Symptom Information:
Symptom ID: | HPO:0008221 | ||||||||||||||||||||||||||
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) Adrenal hyperplasia(HPO:0008221) MedDRA: Vascular disorders(MedDRA:10047065) Vascular hypertensive disorders(MedDRA:10057166) Endocrine and metabolic secondary hypertension(MedDRA:10052741) Adrenal hyperplasia(HPO:0008221) Metabolism and nutrition disorders(MedDRA:10027433) Metabolism disorders NEC(MedDRA:10000546) Metabolic disorders NEC(MedDRA:10027428) Adrenal hyperplasia(HPO:0008221) |
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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) |