ICD-10 · PDGM grouping

Q50-Q56 — Congenital malformations of genital organs

Every ICD-10-CM code in this range and the PDGM clinical group CMS assigns to it, read from the CMS grouper crosswalk v07.1.26.

OASIS-E2 v1.00.0 · ingested 2026-04-26

Codes in range

91

No clinical group

8

A period cannot be grouped from these.

Barred as primary

0

CMS rejects these in the primary position.

Where these codes group

83 of the 91 codes in Q50-Q56 group to MMTA - Other. A further 8 are assigned no clinical group at all, which means a 30-day period cannot be grouped from them.

Every code in Q50-Q56

Descriptions are CMS’s own, abbreviated as CMS abbreviates them.

CodeDescriptionClinical groupPrimary position
Q5001Congenital absence of ovary, unilateralAAccepted
Q5002Congenital absence of ovary, bilateralAAccepted
Q501Developmental ovarian cystAAccepted
Q502Congenital torsion of ovaryAAccepted
Q5031Accessory ovaryAAccepted
Q5032Ovarian streakAAccepted
Q5039Other congenital malformation of ovaryAAccepted
Q504Embryonic cyst of fallopian tubeAAccepted
Q505Embryonic cyst of broad ligamentAAccepted
Q506Oth congenital malformations of fallop and broad ligamentAAccepted
Q510Agenesis and aplasia of uterusAAccepted
Q5110Doubling of uterus w doubling of cervix and vagina w/o obstAAccepted
Q5111Doubling of uterus w doubling of cervix and vagina w obstAAccepted
Q5121Complete doubling of uterusAAccepted
Q5122Partial doubling of uterusAAccepted
Q5128Other and unspecified doubling of uterusAAccepted
Q513Bicornate uterusAAccepted
Q514Unicornate uterusAAccepted
Q515Agenesis and aplasia of cervixAAccepted
Q516Embryonic cyst of cervixAAccepted
Q517Congen fistulae betw uterus and digestive and urinary tractsAAccepted
Q51810Arcuate uterusAAccepted
Q51811Hypoplasia of uterusAAccepted
Q51818Other congenital malformations of uterusAAccepted
Q51820Cervical duplicationAAccepted
Q51821Hypoplasia of cervixAAccepted
Q51828Other congenital malformations of cervixAAccepted
Q519Congenital malformation of uterus and cervix, unspecifiedNoneCannot group
Q520Congenital absence of vaginaAAccepted
Q5210Doubling of vagina, unspecifiedAAccepted
Q5211Transverse vaginal septumAAccepted
Q52120Longitudinal vaginal septum, nonobstructingAAccepted
Q52121Longitudinal vaginal septum, obstructing, right sideAAccepted
Q52122Longitudinal vaginal septum, obstructing, left sideAAccepted
Q52123Longitudinal vaginal septum, microperforate, right sideAAccepted
Q52124Longitudinal vaginal septum, microperforate, left sideAAccepted
Q52129Other and unspecified longitudinal vaginal septumAAccepted
Q522Congenital rectovaginal fistulaAAccepted
Q523Imperforate hymenAAccepted
Q524Other congenital malformations of vaginaAAccepted
Q525Fusion of labiaAAccepted
Q526Congenital malformation of clitorisAAccepted
Q5270Unspecified congenital malformations of vulvaNoneCannot group
Q5271Congenital absence of vulvaAAccepted
Q5279Other congenital malformations of vulvaAAccepted
Q528Other specified congenital malformations of female genitaliaAAccepted
Q529Congenital malformation of female genitalia, unspecifiedNoneCannot group
Q5300Ectopic testis, unspecifiedNoneCannot group
Q5301Ectopic testis, unilateralAAccepted
Q5302Ectopic testes, bilateralAAccepted
Q5310Unspecified undescended testicle, unilateralNoneCannot group
Q53111Unilateral intraabdominal testisAAccepted
Q53112Unilateral inguinal testisAAccepted
Q5312Ectopic perineal testis, unilateralAAccepted
Q5313Unilateral high scrotal testisAAccepted
Q5320Undescended testicle, unspecified, bilateralAAccepted
Q53211Bilateral intraabdominal testesAAccepted
Q53212Bilateral inguinal testesAAccepted
Q5322Ectopic perineal testis, bilateralAAccepted
Q5323Bilateral high scrotal testesAAccepted
Q539Undescended testicle, unspecifiedNoneCannot group
Q540Hypospadias, balanicAAccepted
Q541Hypospadias, penileAAccepted
Q542Hypospadias, penoscrotalAAccepted
Q543Hypospadias, perinealAAccepted
Q544Congenital chordeeAAccepted
Q548Other hypospadiasAAccepted
Q549Hypospadias, unspecifiedAAccepted
Q550Absence and aplasia of testisAAccepted
Q551Hypoplasia of testis and scrotumAAccepted
Q5520Unspecified congenital malformations of testis and scrotumNoneCannot group
Q5521PolyorchismAAccepted
Q5522Retractile testisAAccepted
Q5523Scrotal transpositionAAccepted
Q5529Other congenital malformations of testis and scrotumAAccepted
Q553Atresia of vas deferensAAccepted
Q554Oth congen malform of vas def,epidid, semnl vescl & prostateAAccepted
Q555Congenital absence and aplasia of penisAAccepted
Q5561Curvature of penis (lateral)AAccepted
Q5562Hypoplasia of penisAAccepted
Q5563Congenital torsion of penisAAccepted
Q5564Hidden penisAAccepted
Q5569Other congenital malformation of penisAAccepted
Q557Congenital vasocutaneous fistulaAAccepted
Q558Oth congenital malformations of male genital organsAAccepted
Q559Congenital malformation of male genital organ, unspecifiedNoneCannot group
Q560Hermaphroditism, not elsewhere classifiedAAccepted
Q561Male pseudohermaphroditism, not elsewhere classifiedAAccepted
Q562Female pseudohermaphroditism, not elsewhere classifiedAAccepted
Q563Pseudohermaphroditism, unspecifiedAAccepted
Q564Indeterminate sex, unspecifiedAAccepted

Source: CMS HH PPS Grouper Software v07.1.26, effective 2026-04-01. 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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