Hyperthyroidism
Symptom Information:
Symptom ID: | HPO:0000836 | |||||||||||||||||||||||||
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 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) |
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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) |