Adverse Drug Reaction Classification System

ADR Ontology
ADR Term Congenital hypothyroidism
ADR ID BADD_A01035
ADR Hierarchy
03      Congenital, familial and genetic disorders
03.09      Endocrine disorders congenital
03.09.03      Thyroid disorders congenital
03.09.03.001      Congenital hypothyroidism
05      Endocrine disorders
05.02      Thyroid gland disorders
05.02.03      Thyroid hypofunction disorders
05.02.03.004      Congenital hypothyroidism
14      Metabolism and nutrition disorders
14.11      Metabolism disorders NEC
14.11.01      Metabolic disorders NEC
14.11.01.027      Congenital hypothyroidism
Description A condition in infancy or early childhood due to an in-utero deficiency of THYROID HORMONES that can be caused by genetic or environmental factors, such as thyroid dysgenesis or HYPOTHYROIDISM in infants of mothers treated with THIOURACIL during pregnancy. Endemic cretinism is the result of iodine deficiency. Clinical symptoms include severe MENTAL RETARDATION, impaired skeletal development, short stature, and MYXEDEMA. [MeSH]
MedDRA Code 10010510
MeSH ID D003409; D050033
ADR Severity Grade (FAERS) Not Available
ADR Severity Grade (CTCAE) Not Available
Synonym
Congenital hypothyroidism | Cretinism | Hypothyroidism congenital | Thyroid hypoplasia | Peripheral hypothyroidism | Congenital Hypothyroidism | Hypothyroidism, Congenital | Endemic Cretinism | Cretinism, Endemic | Fetal Iodine Deficiency Disorder | Myxedema, Congenital
Drugs Leading to the ADR
Drug IDDrug NameADR Frequency (FAERS)ADR Severity Grade (FAERS)
BADD_D01095Hydrogen iodide--
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