Hyperthyroidism

Symptom Information:

Symptom ID: HPO:0000836
Synonyms:
Hyperthyroidism (disorder) [Orphanet:41240]
Hyperthyroidism [Orphanet:41240]
Hyperthyroidism [OMIM:Hyperthyroidism]
Hyperthyroidy [Orphanet:41240]
Hyperthyroidism [MedDRA:10020850]
Hyperthyroidism aggravated [MedDRA:10020850]
Thyrotoxicosis [MedDRA:10020850]
Thyrotoxicosis aggravated [MedDRA:10020850]
Thyrotoxicosis from ectopic thyroid nodule [MedDRA:10020850]
Thyrotoxicosis from ectopic thyroid nodule without mention of thyrotoxic crisis or storm [MedDRA:10020850]
Thyrotoxicosis of other specified origin [MedDRA:10020850]
Thyrotoxicosis of other specified origin without mention of thyrotoxic crisis or storm [MedDRA:10020850]
Thyrotoxicosis with goitre [MedDRA:10020850]
Thyrotoxicosis with or without goiter [MedDRA:10020850]
Thyrotoxicosis with or without goitre [MedDRA:10020850]
Thyrotoxicosis without goitre [MedDRA:10020850]
Thyrotoxicosis without mention of goiter or other cause [MedDRA:10020850]
Thyrotoxicosis without mention of goiter or other cause, and w/o ment of thyrotoxic crisis or storm [MedDRA:10020850]
Thyrotoxicosis without mention of goitre or other cause [MedDRA:10020850]
Latent hyperthyroidism [MedDRA:10020850]
Iodine hyperthyroidism [MedDRA:10020850]
Subclinical hyperthyroidism [MedDRA:10020850]
Thyrotoxicosis with goiter [MedDRA:10020850]
Thyrotoxicosis without goiter [MedDRA:10020850]
Thyrotoxicosis [OMIM:Thyrotoxicosis]
Quality:
Cross references:
Orphanet:41240 "Hyperthyroidy" [Orphanet:41240]
OMIM: "Hyperthyroidism" [OMIM:Hyperthyroidism]
OMIM: "Thyrotoxicosis" [OMIM:Thyrotoxicosis]
UMLS:C0020550 "Hyperthyroidism" [HPO:0000836]
UMLS:C0020550 "Hyperthyroidism" [Orphanet:41240]
Is a (Direct Parents):
Orphanet Abnormality of the thyroid gland
HPO         Abnormality of thyroid physiology
MedDRA Thyroid hyperfunction disorders
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the endocrine system(HPO:0000818)
          Abnormality of the thyroid gland(HPO:0000820)
             Abnormality of thyroid physiology(HPO:0002926)
                Hyperthyroidism(HPO:0000836)
MedDRA:
Endocrine disorders(MedDRA:10014698)
    Thyroid gland disorders(MedDRA:10043739)
       Thyroid hyperfunction disorders(MedDRA:10043740)
          Hyperthyroidism(HPO:0000836)
Database Frequency: 25 / 7739
Resource:

All diseases associated with this symptom:

22q11.2 deletion syndrome (Orphanet:567)
Acro-cardio-facial syndrome (Orphanet:2008)
Albright hereditary osteodystrophy (Orphanet:665)
Autoimmune polyendocrinopathy type 2 (Orphanet:3143)
COWDEN SYNDROME 5 (OMIM:615108)
COWDEN SYNDROME 6 (OMIM:615109)
Cowden syndrome (Orphanet:201)
Familial gestational hyperthyroidism (Orphanet:99819)
Familial hyperthyroidism due to mutations in TSH receptor (Orphanet:424)
Fibrous dysplasia of bone (Orphanet:249)
GRAVES DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:275000)
Glutaric acidemia type 3 (Orphanet:35706)
Hydatidiform mole (Orphanet:99927)
Lhermitte-Duclos disease (Orphanet:65285)
MELAS (Orphanet:550)
MERRF (Orphanet:551)
MYASTHENIA GRAVIS (OMIM:254200)
McCune-Albright syndrome (Orphanet:562)
Mitochondrial DNA deletion syndrome with progressive myopathy (Orphanet:352470)
Polyostotic fibrous dysplasia (Orphanet:93276)
Proteus-like syndrome (Orphanet:2969)
Selective pituitary resistance to thyroid hormone (Orphanet:165994)
THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 1 (OMIM:188580)
THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2 (OMIM:613239)
Thyrotoxic periodic paralysis (Orphanet:79102)