ICD-10 · PDGM grouping
E00 Congenital iodine-deficiency syndrome
All 4 codes in the E00 family, with the PDGM clinical group, comorbidity subgroup and primary-position rule CMS assigns, read from the CMS grouper crosswalk v07.2.26 and the CDC FY2027 code file.
Codes in family
4
Can lead a claim
4
Cannot lead a claim
0
What CMS assigns to E00
All 4 codes group to MMTA - Endocrine (3) and MMTA - Other (1). None of the 4 is assigned a comorbidity subgroup. Every code can lead a claim.
Every code in E00
Descriptions are CDC’s FY2027 wording; where CMS’s grouper abbreviates one, its form is shown beneath.
| Code | Description | Primary position | Clinical group | Comorbidity subgroup |
|---|---|---|---|---|
| E00.0 | Congenital iodine-deficiency syndrome, neurological type | Can lead a claim | A | None |
| E00.1 | Congenital iodine-deficiency syndrome, myxedematous type | Can lead a claim | I | None |
| E00.2 | Congenital iodine-deficiency syndrome, mixed type | Can lead a claim | I | None |
| E00.9 | Congenital iodine-deficiency syndrome, unspecified | Can lead a claim | I | None |
Sources: CMS HH PPS Grouper Software v07.2.26, effective 2026-10-01, for the clinical group, comorbidity subgroup, code-first conventions and primary-position flags; CDC NCHS ICD-10-CM FY2027 code descriptions for the family title and code wording. This is the crosswalk Medicare runs a claim through. Grouping also depends on admission source, timing, the OASIS functional items and the rest of the diagnosis list.
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