Congenital hypothyroidism

Congenital hypothyroidism (disorder)

active

Code	`190268003`
Semantic tag	disorder
Module	international
Definition	defined
Effective time	20140731

Parents (2)

66091009Congenital disease disorder
40930008Hypothyroidism disorder

Children (33)

55838005Athyrotic hypothyroidism sequence disorder
722375007Bamforth Lazarus syndrome disorder
722938007Congenital central hypothyroidism disorder
718690009Congenital hypothyroidism due to absence of thyroid gland disorder
1179404005Congenital hypothyroidism due to congenital anomaly of thyroid gland disorder
1179400001Congenital hypothyroidism due to dual oxidase maturation factor 2 disorder
722939004Congenital hypothyroidism due to iodine deficiency disorder
783177006Congenital hypothyroidism due to maternal intake of antithyroid drug disorder
1179401002Congenital hypothyroidism due to peripheral resistance to thyroid hormone disorder
1179397005Congenital hypothyroidism due to symporter mutation disorder
1179399008Congenital hypothyroidism due to thyroglobulin mutation disorder
1179396001Congenital hypothyroidism due to thyroid deiodinase mutation disorder
1179394003Congenital hypothyroidism due to thyroid peroxidase mutation disorder
717333002Congenital hypothyroidism due to transplacental passage of maternal thyroid stimulating hormone binding inhibitory antibody disorder
278503003Congenital hypothyroidism with diffuse goitre disorder
237515009Congenital hypothyroidism without goitre disorder
190304001Dyshormonogenic goitre disorder
718183003Familial thyroid dyshormonogenesis disorder
770631009Genetic transient congenital hypothyroidism disorder
56041007Hypothyroidism due to defect in thyroid hormone synthesis disorder
237555006Hypothyroidism due to iodide trapping defect disorder
718194004Hypothyroidism due to mutation in transcription factor of pituitary development disorder
717334008Idiopathic congenital hypothyroidism disorder
52724003Iodide oxidation defect disorder
22558005Iodide transport defect disorder
64491003Myxoedematous form of cretinism disorder
206457007Neonatal jaundice with congenital hypothyroidism disorder
722051004Obesity, colitis, hypothyroidism, cardiac hypertrophy, developmental delay syndrome disorder
699298009Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant disorder
1260240000Resistance to thyroid hormone due to mutation in thyroid hormone receptor alpha disorder
763890006Short stature with delayed bone age due to thyroid hormone metabolism deficiency disorder
84781002Sporadic cretinism disorder
1142106007Transient congenital hypothyroidism due to dual oxidase 2 mutation disorder