Growth hormone excess

Symptom Information:

Symptom ID: HPO:0000845
Synonyms:
Acral hypertrophy [HPO:0000845]
Acromegalic growth [HPO:0000845]
Acromegaly [HPO:0000845]
Acromegaly [Orphanet:53300]
Acromegaly (disorder) [Orphanet:53300]
Acromegaly [OMIM:Acromegaly]
Acromegaly [MedDRA:10000599]
Acromegaly and gigantism [MedDRA:10000599]
Acral overgrowth [MedDRA:10000599]
Quality:
Cross references:
Orphanet:53300 "Acromegaly" [Orphanet:53300]
OMIM: "Acromegaly" [OMIM:Acromegaly]
UMLS:C0001206 "Acromegaly" [HPO:0000845]
UMLS:C0001206 "Acromegaly" [Orphanet:53300]
Is a (Direct Parents):
HPO         Hyperpituitarism
Orphanet Build/stature/longevity anomalies
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 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)
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)