Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Decreased circulating T4 concentration
Always present (100%)HP:0031507
Decreased thyrotropin level
Always present (100%)HP:0031098
Hypothyroidism
Always present (100%)HP:0000821
Depressed nasal root/bridge
Frequent (30-79%)HP:0005280
Dry skin
Frequent (30-79%)HP:0000958
Feeding difficulties
Frequent (30-79%)HP:0011968
Hoarse cry
Frequent (30-79%)HP:0001615
Lingual hyperplasia
Frequent (30-79%)HP:0000158
No development of motor milestones
Frequent (30-79%)HP:0001270
Omphalocoele
Frequent (30-79%)HP:0001539
Wider-than-typical soft spot of skull
Frequent (30-79%)HP:0000260
Low intelligence
HP:0001249
Marked growth retardation
HP:0008850
Mental retardation, severe
HP:0010864
Peripheral hypotonia
HP:0001252
Umbilical hernia
HP:0001537
Quick Facts
- SNOMED CT
- 82598004
- UMLS CUI
- C3665349
- Fully Specified Name
- Secondary hypothyroidism (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.