Overview
Genetic transient congenital hypothyroidism 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.
Decreased circulating T4 concentration
Frequent (30-79%)HP:0031507
Increased circulating thyroglobulin concentration
Frequent (30-79%)HP:0025484
Thyroid defect in oxidation and organification of iodide
Frequent (30-79%)HP:0008263
Thyroid goiter
Frequent (30-79%)HP:0000853
Thyroid-stimulating hormone excess
Frequent (30-79%)HP:0002925
Abnormal radioactive iodine uptake test result
Occasional (5-29%)HP:0031221
Dyschezia
Occasional (5-29%)HP:0002019
Excessive daytime somnolence
Occasional (5-29%)HP:0001262
Feeding difficulties
Occasional (5-29%)HP:0011968
Hoarse cry
Occasional (5-29%)HP:0001615
Languor
Occasional (5-29%)HP:0001254
Lingual hyperplasia
Occasional (5-29%)HP:0000158
Mottled pigmentation
Occasional (5-29%)HP:0001070
Postterm pregnancy
Occasional (5-29%)HP:0031169
Prolonged neonatal jaundice
Occasional (5-29%)HP:0006579
Umbilical hernia
Occasional (5-29%)HP:0001537
Central hypotonia
Very rare (1-4%)HP:0001252
Edema
Very rare (1-4%)HP:0000969
Hypothermia
Very rare (1-4%)HP:0002045
Small thyroid gland
Very rare (1-4%)HP:0005990
Related Conditions
Quick Facts
- SNOMED CT
- 770631009
- UMLS CUI
- C4749351
- Fully Specified Name
- Genetic transient congenital hypothyroidism (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 20
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.