Congenital disease	Hypothyroidism
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Congenital hypothyroidism (disorder)
	Congenital hypothyroidism
	congenitale hypothyreoïdie
	congenitale hypothyroïdie
	congenitale hypothyreoïdie
	congenitale hypothyroïdie
	CHT; aangeboren afwijking met een verminderde schildklierwerking of het ontbreken van de schildklier.

Id	190268003
Status	Defined

Finding site	Thyroid structure
Occurrence	Congenital

General Practice / Family Practice reference set

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	E03.1
Rule	TRUE
Advice	ALWAYS E03.1
Correlation	SNOMED CT source code to target map code correlation not specified

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Athyrotic hypothyroidism sequence

Bamforth Lazarus syndrome

Congenital central hypothyroidism1

Congenital hypothyroidism due to absence of thyroid gland

Congenital hypothyroidism due to congenital anomaly of thyroid gland

Congenital hypothyroidism due to dual oxidase maturation factor 2

Congenital hypothyroidism due to iodine deficiency

Congenital hypothyroidism due to maternal intake of antithyroid drug

Congenital hypothyroidism due to peripheral resistance to thyroid hormone

Congenital hypothyroidism due to symporter mutation

Congenital hypothyroidism due to thyroglobulin mutation

Congenital hypothyroidism due to thyroid deiodinase mutation

Congenital hypothyroidism due to thyroid peroxidase mutation

Congenital hypothyroidism due to transplacental passage of maternal thyroid stimulating hormone binding inhibitory antibody

Congenital hypothyroidism with diffuse goiter

Congenital hypothyroidism without goiter1

Dyshormonogenic goiter5

Familial thyroid dyshormonogenesis

Genetic transient congenital hypothyroidism

Hypothyroidism due to defect in thyroid hormone synthesis1

Hypothyroidism due to iodide trapping defect

Hypothyroidism due to mutation in transcription factor of pituitary development

Idiopathic congenital hypothyroidism

Iodide oxidation defect

Iodide transport defect

Myxedematous form of cretinism1

Neonatal jaundice with congenital hypothyroidism

Obesity, colitis, hypothyroidism, cardiac hypertrophy, developmental delay syndrome

Obesity, colitis, hypothyroidism, cardiac hypertrophy, developmental delay syndrome

Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant

Short stature with delayed bone age due to thyroid hormone metabolism deficiency

Sporadic cretinism

Thyroid hormone responsiveness defect4

Transient congenital hypothyroidism due to dual oxidase 2 mutation