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Resistance to thyrotropin-releasing hormone syndrome
disorderSNOMED 725462002CUI C1861106
Overview
Resistance to thyrotropin-releasing hormone syndrome 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.
Abnormal circulating thyroglobulin concentration
Frequent (30-79%)HP:0025483
Abnormality of the nervous system
Frequent (30-79%)HP:0000707
Decreased circulating free T3
Frequent (30-79%)HP:0032210
Decreased circulating T4 concentration
Frequent (30-79%)HP:0031507
Delayed skeletal development
Frequent (30-79%)HP:0002750
Depressive episode
Frequent (30-79%)HP:0000716
Growth failure
Frequent (30-79%)HP:0001510
Husky voice
Frequent (30-79%)HP:0001609
Inactivity
Frequent (30-79%)HP:0001254
Neurodevelopmental delay
Frequent (30-79%)HP:0012758
Overweight
Frequent (30-79%)HP:0025502
Prolactin excess
Frequent (30-79%)HP:0000870
Prolonged neonatal jaundice
Frequent (30-79%)HP:0006579
Reduced circulating prolactin concentration
Frequent (30-79%)HP:0008202
Reduced radioactive iodine uptake
Frequent (30-79%)HP:0031219
Small thyroid gland
Frequent (30-79%)HP:0005990
Tiredness
Frequent (30-79%)HP:0012378
TSH deficient hypothyroidism
Frequent (30-79%)HP:0008245
Xerosis
Frequent (30-79%)HP:0000958
Decreased body height
HP:0004322
Reduced TSH response to thyrotrophin-releasing hormone stimulation test
HP:0033082
Quick Facts
- SNOMED CT
- 725462002
- UMLS CUI
- C1861106
- Fully Specified Name
- Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 21
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.