Growth hormone excess
Symptom Information:
Symptom ID: | HPO:0000845 | |||||||||
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 hypothalamus-pituitary axis(HPO:0000864) Abnormality of the pituitary gland(HPO:0012503) Abnormality of the anterior pituitary(HPO:0011747) Hyperpituitarism(HPO:0010514) Growth hormone excess(HPO:0000845) MedDRA: Vascular disorders(MedDRA:10047065) Vascular hypertensive disorders(MedDRA:10057166) Endocrine and metabolic secondary hypertension(MedDRA:10052741) Growth hormone excess(HPO:0000845) |
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Database Frequency: | 18 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
Acromegaly | (Orphanet:963) |
Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
CARNEY COMPLEX, TYPE 1 | (OMIM:160980) |
CHROMOSOME Xq26.3 DUPLICATION SYNDROME | (OMIM:300942) |
Carney complex | (Orphanet:1359) |
Familial isolated pituitary adenoma | (Orphanet:314777) |
Fibrous dysplasia of bone | (Orphanet:249) |
Gigantism | (Orphanet:99725) |
Insulin-resistance syndrome type A | (Orphanet:2297) |
Leprechaunism | (Orphanet:508) |
McCune-Albright syndrome | (Orphanet:562) |
Multiple endocrine neoplasia type 1 | (Orphanet:652) |
Multiple endocrine neoplasia type 4 | (Orphanet:276152) |
PITUITARY ADENOMA, GROWTH HORMONE-SECRETING, 2 | (OMIM:300943) |
Pachydermoperiostosis | (Orphanet:2796) |
Polyostotic fibrous dysplasia | (Orphanet:93276) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Somatotroph adenoma | (Orphanet:96256) |