Overview
Familial gestational hyperthyroidism is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Activating TSHR defect
Always present (100%)HP:0011790
Decreased thyrotropin level
Always present (100%)HP:0031098
Hyperthyroidism
Always present (100%)HP:0000836
Increased circulating T4 concentration
Always present (100%)HP:0031506
Racing heart
Always present (100%)HP:0001649
Diarrhea
Very frequent (80-99%)HP:0002014
Thyroid goiter
Very frequent (80-99%)HP:0000853
Thyroid hyperplasia
Very frequent (80-99%)HP:0008249
Thyrotoxicosis with diffuse goiter
Very frequent (80-99%)HP:0011784
tremors in hands
Very frequent (80-99%)HP:0002378
Weight loss
Very frequent (80-99%)HP:0001824
Delayed motor milestones
Frequent (30-79%)HP:0001270
hyperkinetic disorder
Frequent (30-79%)HP:0000752
Psychomotor agitation
Frequent (30-79%)HP:0000713
Trouble sleeping
Frequent (30-79%)HP:0002360
Protruding eyes
Occasional (5-29%)HP:0000520
Related Conditions
Quick Facts
- SNOMED CT
- 703309000
- UMLS CUI
- C1863959
- Fully Specified Name
- Familial gestational hyperthyroidism (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 16
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.