5A00.04ICD-11 MMS 2026-01
Congenital hypothyroidism due to iodine deficiency
Description
Hypothyroidism is a condition which arises at birth where the thyroid gland produces too little or no thyroid hormone and it can be induced by iodine-deficiency.
Index terms
- Congenital hypothyroidism due to iodine deficiency
- Congenital iodine-deficiency hypothyroidism NOS
- congenital iodine-deficiency syndrome
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- fetal iodine deficiency syndrome
- Arthropathy in congenital iodine-deficiency syndrome
- Congenital iodine-deficiency syndrome, neurological type
- Endemic hypothyroidism, neurological type
- endemic cretinism - neurological type
- neurological cretin
- Congenital iodine-deficiency syndrome, myxoedematous type
- Endemic hypothyroidism, myxoedematous type
- congenital iodine deficiency syndrome - myxoedematous type
- congenital myxoedema
- congenital myxoedema coma
- endemic congenital iodine deficiency syndrome of myxoedematous type
- endemic cretinism - myxoedematous type
- hypothyroid cretin
- hypothyroid endemic cretinism
- hypothyroid endemic hypothyroidism
- myxoedematous cretin
- myxoedematous form of cretinism
- Congenital iodine-deficiency syndrome, mixed type
- Endemic hypothyroidism, mixed type
- mixed cretin
- mixed type endemic cretinism
Excludes
5A00.22– Subclinical iodine-deficiency hypothyroidism
Exclusions from above levels
18– Pregnancy, childbirth or the puerperium- http://id.who.int/icd/entity/1004987305 – Transitory endocrine or metabolic disorders specific to fetus or newborn
Sibling codes
Foundation entity
Congenital hypothyroidism due to iodine deficiency – http://id.who.int/icd/entity/900488632
Allowed postcoordination axes
Part of: 5A00.0: Congenital hypothyroidism › 5A00: Hypothyroidism › 05: Endocrine, nutritional or metabolic diseases