Category · FY2027
E00 Congenital iodine-deficiency syndrome
- Header · not billable
E00 is not billable. The category heads 4 billable codes in FY2027: the 4 codes directly below it.
Index → code
Where it sits
- Chapter 4 Endocrine, nutritional and metabolic diseases (E00-E89)
- E00-E07 Disorders of thyroid gland (E00-E07)
- E00 Congenital iodine-deficiency syndrome
- Billable codes
- 4
- Subdivisions
- 4
- CC / MCC codes
- 0 / 0
- HCC V28 codes
- 0
- New FY2027
- 0
- Index entries
- 11
Codes in E00
- E00.0Congenital iodine-deficiency syndrome, neurological typeBillable
Inclusion terms 1
Inclusion terms
- Endemic cretinism, neurological type
- E00.1Congenital iodine-deficiency syndrome, myxedematous typeBillable
Inclusion terms 2
Inclusion terms
- Endemic hypothyroid cretinism
- Endemic cretinism, myxedematous type
- E00.2Congenital iodine-deficiency syndrome, mixed typeBillable
Inclusion terms 1
Inclusion terms
- Endemic cretinism, mixed type
- E00.9Congenital iodine-deficiency syndrome, unspecifiedBillable
Inclusion terms 2
Inclusion terms
- Congenital iodine-deficiency hypothyroidism NOS
- Endemic cretinism NOS
Instructions
At E00
Excludes1
- subclinical iodine-deficiency hypothyroidism (E02) E02
Notes that also apply
Chapter 4 instructions (Notes 1, Excludes1 1): printed on the chapter 4 page.
Index entries
- Cretin, cretinism (congenital) (endemic) (nongoitrous) (sporadic) → E00.9
- Myxedema (adult) (idiocy) (infantile) (juvenile)›congenital → E00.1
- Syndrome›iodine-deficiency, congenital → E00.9
- Cretin, cretinism (congenital) (endemic) (nongoitrous) (sporadic)›type›neurological → E00.0
- Cretin, cretinism (congenital) (endemic) (nongoitrous) (sporadic)›type›hypothyroid → E00.1
- Cretin, cretinism (congenital) (endemic) (nongoitrous) (sporadic)›type›myxedematous → E00.1
- Cretin, cretinism (congenital) (endemic) (nongoitrous) (sporadic)›type›mixed → E00.2
- Myopathy›in (due to)›cretinism → E00.9 [G73.7]
- Syndrome›iodine-deficiency, congenital›type›neurological → E00.0
- Syndrome›iodine-deficiency, congenital›type›myxedematous → E00.1
- Syndrome›iodine-deficiency, congenital›type›mixed → E00.2
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