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Home/Diagnosis/ICD-10 Coding for Congenital Hypertrophy of Retinal Pigment Epithelium

ICD-10 Coding for Congenital Hypertrophy of Retinal Pigment Epithelium

Q14.1
D12.6

Complete ICD-10-CM coding and documentation guide for icd-10 coding for congenital hypertrophy of retinal pigment epithelium includes clinical validation requirements, medical necessity guidelines, and coding policies.

Also Known as:
CHRPE
Retinal Pigment Hypertrophy
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Key Information: ICD-10 Coding for Congenital Hypertrophy of Retinal Pigment Epithelium

Essential facts and insights about ICD-10 Coding for Congenital Hypertrophy of Retinal Pigment Epithelium

Use ICD-10 code Q14.1 for congenital malformation of retina, ensuring proper documentation in clinical notes.

Primary ICD-10-CM Codes

Congenital malformation of retina

Billable Code
Q14.1
Billable

Diagnostic Criteria

clinical:
  • • Presence of pigmented retinal lesions with typical CHRPE appearance
documentation:
  • • Detailed description of lesion characteristics and any family history of FAP

Applicable To

  • • Solitary CHRPE
  • • Atypical CHRPE

Important Notes

  • • Ensure documentation specifies lesion characteristics and any genetic testing results.

Adenomatous polyposis of colon

Billable Code
D12.6
Billable

Diagnostic Criteria

clinical:
  • • Genetic testing confirming APC mutation
  • • Colonoscopy findings of multiple adenomatous polyps

Applicable To

  • • Familial Adenomatous Polyposis

Important Notes

  • • Sequence D12.6 first if the encounter is primarily for FAP management.
Ancillary Codes

Additional codes that may be used with this diagnosis

Z84.81

Family history of colonic polyps

Use to indicate family history when FAP is suspected but not confirmed.

Frequently Asked Questions

What is the ICD-10 code for CHRPE?

The ICD-10 code for Congenital Hypertrophy of Retinal Pigment Epithelium (CHRPE) is Q14.1. If associated with Familial Adenomatous Polyposis (FAP), use D12.6 as well.

How is CHRPE related to FAP coded?

When CHRPE is associated with FAP, use Q14.1 for CHRPE and D12.6 for FAP. Ensure documentation includes genetic testing results.

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