Congenitale hypothyreoïdie
Een tekort aan schildklierhormoon dat al vanaf de geboorte aanwezig is.
Geanalyseerde genen
Ook bekend als
congenital goitre; congenital iodine deficiency syndrome; cretinism; foetal iodine deficiency syndrome
Bevat 35 gerelateerde subtypen ↓Subtypen verbergen ↑
- central congenital hypothyroidism
- congenital hypothyroidism due to maternal intake of antithyroid drugs
- congenital hypothyroidism due to transplacental passage of maternal TSH-binding inhibitory antibodies
- congenital nongoitrous hypothyroidism 3
- congenital nongoitrous hypothyroidism 6
- familial thyroid dyshormonogenesis
- fetal iodine syndrome
- hypothyroidism due to deficient transcription factors involved in pituitary development or function
- hypothyroidism due to iodide transport defect
- hypothyroidism due to TSH receptor mutations
- hypothyroidism, congenital, nongoitrous
- hypothyroidism, congenital, nongoitrous, 2
- hypothyroidism, congenital, nongoitrous, 5
- hypothyroidism, congenital, nongoitrous, 7
- hypothyroidism, congenital, nongoitrous, 8
- hypothyroidism, congenital, nongoitrous, 9
- idiopathic congenital hypothyroidism
- isolated thyroid-stimulating hormone deficiency
- isolated thyrotropin-releasing hormone deficiency
- Kocher-debre-Semelaigne syndrome
- Pendred syndrome
- peripheral hypothyroidism
- peripheral resistance to thyroid hormones
- permanent congenital hypothyroidism
- thyroid dyshormonogenesis 1
- thyroid dyshormonogenesis 2A
- thyroid dyshormonogenesis 3
- thyroid dyshormonogenesis 4
- thyroid dyshormonogenesis 5
- thyroid dyshormonogenesis 6
- thyroid hormone metabolism, abnormal 1
- transient congenital hypothyroidism
- transient congenital hypothyroidism due to maternal factor
- transient congenital hypothyroidism due to neonatal factor
- X-linked central congenital hypothyroidism with late-onset testicular enlargement
