Thyroid-stimulating hormone excess

Symptom Information:

Symptom ID: HPO:0002925
Synonyms:
Elevated thyroid stimulating hormone [HPO:0002925]
Elevated thyroid stimulating hormone levels [HPO:0002925]
High TSH [HPO:0002925]
Increased serum thyroid-stimulating hormone [HPO:0002925]
Increased thyroid-stimulating hormone [HPO:0002925]
TSH excess [HPO:0002925]
High TSH [OMIM:High TSH]
Elevated thyroid stimulating hormone (188540) levels [OMIM:Elevated thyroid stimulating hormone (188540) levels]
Elevated thyroid stimulating hormone (TSH) [OMIM:Elevated thyroid stimulating hormone (TSH)]
Increased serum thyroid-stimulating hormone (TSH) [OMIM:Increased serum thyroid-stimulating hormone (TSH)]
Increased thyroid-stimulating hormone (TSH) [OMIM:Increased thyroid-stimulating hormone (TSH)]
Quality:
Cross references:
OMIM: "High TSH" [OMIM:High TSH]
OMIM: "Elevated thyroid stimulating hormone (188540) levels" [OMIM:Elevated thyroid stimulating hormone (188540) levels]
OMIM: "Elevated thyroid stimulating hormone (TSH)" [OMIM:Elevated thyroid stimulating hormone (TSH)]
OMIM: "Increased serum thyroid-stimulating hormone (TSH)" [OMIM:Increased serum thyroid-stimulating hormone (TSH)]
OMIM: "Increased thyroid-stimulating hormone (TSH)" [OMIM:Increased thyroid-stimulating hormone (TSH)]
Is a (Direct Parents):
HPO         Hyperpituitarism
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)
                      Thyroid-stimulating hormone excess(HPO:0002925)
MedDRA:
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

Acro-osteolysis-keloid-like lesions-premature aging syndrome (Orphanet:363665)
Allan-Herndon-Dudley syndrome (Orphanet:59)
Brain-lung-thyroid syndrome (Orphanet:209905)
Hypothyroidism due to TSH receptor mutations (Orphanet:90673)
MYXEDEMA (OMIM:255900)
Microcephaly-capillary malformation syndrome (Orphanet:294016)
Schimke immuno-osseous dysplasia (Orphanet:1830)
Selective pituitary resistance to thyroid hormone (Orphanet:165994)
Short stature-delayed bone age due to thyroid hormone metabolism deficiency (Orphanet:171706)
Thyroid ectopia (Orphanet:95712)
Thyroid hemiagenesis (Orphanet:95719)
Woodhouse-Sakati syndrome (Orphanet:3464)