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E00.1 - Congenital iodine-deficiency syndrome, myxedematous type


The ICD 10 Code for Congenital iodine-deficiency syndrome, myxedematous type is listed as E00.1.
Additional information concerning this code and description can be found below including ICD 9 crosswalks / GEMS, chapter information, and DRGs where available.

ICD 10 CM Field Value
Diagnosis Code: E00.1
Description: Congenital iodine-deficiency syndrome, myxedematous type
  • Endemic hypothyroid cretinism
  • Endemic cretinism, myxedematous type
Diagnostic Related Groups
(MS-DRG v30.0)
643 - Endocrine Disorders W Mcc
644 - Endocrine Disorders W Cc
645 - Endocrine Disorders W/o Cc/mcc
Chapter Endocrine, nutritional and metabolic diseases (E00-E89)
Block Disorders of thyroid gland (E00-E07)
Parent E00 - Congenital iodine-deficiency syndrome
ICD-9-CM Diagnosis Codes General Equivalence Mappings (GEMS):
ICD 9 Dx Code: 243 - Congenital hypothyroidism (approximate)
ICD-10-CM Siblings (same level / similar specificity) of E00.1:
E00.0 - Congenital iodine-deficiency syndrome, neurological type
E00.2 - Congenital iodine-deficiency syndrome, mixed type
E00.9 - Congenital iodine-deficiency syndrome, unspecified