Overview
Idiopathic 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
Very frequent (80-99%)HP:0031507
Thyroid-stimulating hormone excess
Very frequent (80-99%)HP:0002925
Anomaly of the epiphyses
Frequent (30-79%)HP:0005930
Delayed closure of the fontanelles
Frequent (30-79%)HP:0000270
Delayed ossification proximal femoral epiphyses
Frequent (30-79%)HP:0008828
Dyschezia
Frequent (30-79%)HP:0002019
Feeding difficulties in infancy
Frequent (30-79%)HP:0008872
Large posterior fontanelle
Frequent (30-79%)HP:0004491
Neurodevelopmental delay
Frequent (30-79%)HP:0012758
Prolonged neonatal jaundice
Frequent (30-79%)HP:0006579
Umbilical hernia
Frequent (30-79%)HP:0001537
Bradycardia
Occasional (5-29%)HP:0001662
Dullness
Occasional (5-29%)HP:0001254
Facial swelling
Occasional (5-29%)HP:0000282
Flat nasal bridge
Occasional (5-29%)HP:0005280
Hyperbilirubinemia, neonatal
Occasional (5-29%)HP:0003265
Hyporeflexia
Occasional (5-29%)HP:0001265
Hypothermia
Occasional (5-29%)HP:0002045
Lingual hyperplasia
Occasional (5-29%)HP:0000158
Peripheral hypotonia
Occasional (5-29%)HP:0001252
Quick Facts
- SNOMED CT
- 717334008
- UMLS CUI
- C4273913
- Fully Specified Name
- Idiopathic 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.