Congenital absence of half of thyroid

disorder

SNOMED 715734006CUI C4023190

Overview

Congenital absence of half of thyroid 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.

Thyroid hemiagenesis

Always present (100%)HP:0011780

Abdominal swelling

Very frequent (80-99%)HP:0003270

Anomaly of the face

Very frequent (80-99%)HP:0000271

Athyroidal hypothyroidism

Very frequent (80-99%)HP:0008191

Cognitive delay

Very frequent (80-99%)HP:0001263

Dyschezia

Very frequent (80-99%)HP:0002019

Excessive daytime somnolence

Very frequent (80-99%)HP:0001262

Growth deficiency

Very frequent (80-99%)HP:0001510

Lingual hyperplasia

Very frequent (80-99%)HP:0000158

Peripheral hypotonia

Very frequent (80-99%)HP:0001252

Thickened facial skin with coarse facial features

Very frequent (80-99%)HP:0000280

Tiredness

Very frequent (80-99%)HP:0012378

Umbilical hernia

Very frequent (80-99%)HP:0001537

Wide bregma sutures

Very frequent (80-99%)HP:0000239

Yellowing of the skin

Very frequent (80-99%)HP:0000952

Anti-thyroid globulin antibody positivity

Frequent (30-79%)HP:0032069

Anti-thyroid peroxidase antibody positivity

Frequent (30-79%)HP:0025379

Hashimoto's thyroiditis

Frequent (30-79%)HP:0000872

Increased circulating free T3

Frequent (30-79%)HP:0011788

Thyroid adenoma

Frequent (30-79%)HP:0000854

Thyroid nodule

Frequent (30-79%)HP:0025388

Thyroid-stimulating hormone excess

Frequent (30-79%)HP:0002925

Graves disease

Occasional (5-29%)HP:0100647

Hyperparathyroidism

Occasional (5-29%)HP:0000843

Papillary carcinoma of thyroid

Occasional (5-29%)HP:0002895

Follicular thyroid carcinoma

Very rare (1-4%)HP:0006731

Medullary thyroid cancer

Very rare (1-4%)HP:0002865

Related Conditions

Congenital absence of thyroid gland(parent)

Quick Facts

SNOMED CT: 715734006
UMLS CUI: C4023190
Fully Specified Name: Congenital absence of half of thyroid (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 27

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.