Q01.9

Encephalocele, unspecified

Risk-adjusting (HCC)Billable code

HCC risk adjustment mapping

CMS-HCC V28

HCC182

Spinal Cord Disorders/Injuries

CMS-HCC ESRD V24

HCC72

Spinal Cord Disorders/Injuries

RxHCC V08

RXHCC155

Spinal Cord Disorders

Coding notes

Excludes 1 never coded together · Excludes 2 may co-exist

Inherited from Q01Encephalocele

Includes

Arnold-Chiari syndrome, type III encephalocystocele encephalomyelocele hydroencephalocele hydromeningocele, cranial meningocele, cerebral meningoencephalocele

Excludes 1

Meckel-Gruber syndrome (Q61.9)

Inherited from chapter 17Congenital malformations, deformations and chromosomal abnormalities

Excludes 2

inborn errors of metabolism (E70-E88)

Note

Codes from this chapter are not for use on maternal records

Official Guidelines for Q01.9

FY 2026 ›

I.C.17Chapter-specific guidanceChapter 17: Congenital malformations, deformations, and chromosomal abnormalities (Q00-QA1)

Sections that reference Q01.9

IV.QEncounters for routine health screeningsOutpatient services
… Congenital conditions and anomalies Assign “Y” for congenital conditions and anomalies except for categories Q00- Q99, Congenital anomalies, which are on the exempt list. …

Sections whose FY 2026 text names Q01.9, its Q01 category, or a range containing it — the chapter guidance above is the authoritative source.

Find Q01.9 in the alphabetic index

3 index paths lead to this code