Genitourinary congenital anomalies

Code Families in This Category

• Q64 Other congenital malformations of urinary system · 22
• Q52 Other congenital malformations of female genitalia · 20
• Q51 Congenital malformations of uterus and cervix · 19
• Q55 Other congenital malformations of male genital organs · 18
• Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter · 17
• Q53 Undescended and ectopic testicle · 16
• Q61 Cystic kidney disease · 11
• Q50 Congenital malformations of ovaries, fallopian tubes and broad ligaments · 10
• Q54 Hypospadias · 7
• Q60 Renal agenesis and other reduction defects of kidney · 7
• Q63 Other congenital malformations of kidney · 6
• Q56 Indeterminate sex and pseudohermaphroditism · 5

ICD-10-CM Codes in This Category (first 100 of 158)

• Q50.01 — Congenital absence of ovary, unilateral
• Q50.02 — Congenital absence of ovary, bilateral
• Q50.1 — Developmental ovarian cyst
• Q50.2 — Congenital torsion of ovary
• Q50.31 — Accessory ovary
• Q50.32 — Ovarian streak
• Q50.39 — Other congenital malformation of ovary
• Q50.4 — Embryonic cyst of fallopian tube
• Q50.5 — Embryonic cyst of broad ligament
• Q50.6 — Other congenital malformations of fallopian tube and broad ligament
• Q51.0 — Agenesis and aplasia of uterus
• Q51.10 — Doubling of uterus with doubling of cervix and vagina without obstruction
• Q51.11 — Doubling of uterus with doubling of cervix and vagina with obstruction
• Q51.2 — Other doubling of uterus
• Q51.21 — Complete doubling of uterus
• Q51.22 — Partial doubling of uterus
• Q51.28 — Other and unspecified doubling of uterus
• Q51.3 — Bicornate uterus
• Q51.4 — Unicornate uterus
• Q51.5 — Agenesis and aplasia of cervix
• Q51.6 — Embryonic cyst of cervix
• Q51.7 — Congenital fistulae between uterus and digestive and urinary tracts
• Q51.810 — Arcuate uterus
• Q51.811 — Hypoplasia of uterus
• Q51.818 — Other congenital malformations of uterus
• Q51.820 — Cervical duplication
• Q51.821 — Hypoplasia of cervix
• Q51.828 — Other congenital malformations of cervix
• Q51.9 — Congenital malformation of uterus and cervix, unspecified
• Q52.0 — Congenital absence of vagina
• Q52.10 — Doubling of vagina, unspecified
• Q52.11 — Transverse vaginal septum
• Q52.12 — Longitudinal vaginal septum
• Q52.120 — Longitudinal vaginal septum, nonobstructing
• Q52.121 — Longitudinal vaginal septum, obstructing, right side
• Q52.122 — Longitudinal vaginal septum, obstructing, left side
• Q52.123 — Longitudinal vaginal septum, microperforate, right side
• Q52.124 — Longitudinal vaginal septum, microperforate, left side
• Q52.129 — Other and unspecified longitudinal vaginal septum
• Q52.2 — Congenital rectovaginal fistula
• Q52.3 — Imperforate hymen
• Q52.4 — Other congenital malformations of vagina
• Q52.5 — Fusion of labia
• Q52.6 — Congenital malformation of clitoris
• Q52.70 — Unspecified congenital malformations of vulva
• Q52.71 — Congenital absence of vulva
• Q52.79 — Other congenital malformations of vulva
• Q52.8 — Other specified congenital malformations of female genitalia
• Q52.9 — Congenital malformation of female genitalia, unspecified
• Q53.00 — Ectopic testis, unspecified
• Q53.01 — Ectopic testis, unilateral
• Q53.02 — Ectopic testes, bilateral
• Q53.10 — Unspecified undescended testicle, unilateral
• Q53.11 — Abdominal testis, unilateral
• Q53.111 — Unilateral intraabdominal testis
• Q53.112 — Unilateral inguinal testis
• Q53.12 — Ectopic perineal testis, unilateral
• Q53.13 — Unilateral high scrotal testis
• Q53.20 — Undescended testicle, unspecified, bilateral
• Q53.21 — Abdominal testis, bilateral
• Q53.211 — Bilateral intraabdominal testes
• Q53.212 — Bilateral inguinal testes
• Q53.22 — Ectopic perineal testis, bilateral
• Q53.23 — Bilateral high scrotal testes
• Q53.9 — Undescended testicle, unspecified
• Q54.0 — Hypospadias, balanic
• Q54.1 — Hypospadias, penile
• Q54.2 — Hypospadias, penoscrotal
• Q54.3 — Hypospadias, perineal
• Q54.4 — Congenital chordee
• Q54.8 — Other hypospadias
• Q54.9 — Hypospadias, unspecified
• Q55.0 — Absence and aplasia of testis
• Q55.1 — Hypoplasia of testis and scrotum
• Q55.20 — Unspecified congenital malformations of testis and scrotum
• Q55.21 — Polyorchism
• Q55.22 — Retractile testis
• Q55.23 — Scrotal transposition
• Q55.29 — Other congenital malformations of testis and scrotum
• Q55.3 — Atresia of vas deferens
• Q55.4 — Other congenital malformations of vas deferens, epididymis, seminal vesicles and prostate
• Q55.5 — Congenital absence and aplasia of penis
• Q55.61 — Curvature of penis (lateral)
• Q55.62 — Hypoplasia of penis
• Q55.63 — Congenital torsion of penis
• Q55.64 — Hidden penis
• Q55.69 — Other congenital malformation of penis
• Q55.7 — Congenital vasocutaneous fistula
• Q55.8 — Other specified congenital malformations of male genital organs
• Q55.9 — Congenital malformation of male genital organ, unspecified
• Q56.0 — Hermaphroditism, not elsewhere classified
• Q56.1 — Male pseudohermaphroditism, not elsewhere classified
• Q56.2 — Female pseudohermaphroditism, not elsewhere classified
• Q56.3 — Pseudohermaphroditism, unspecified
• Q56.4 — Indeterminate sex, unspecified
• Q60.0 — Renal agenesis, unilateral
• Q60.1 — Renal agenesis, bilateral
• Q60.2 — Renal agenesis, unspecified
• Q60.3 — Renal hypoplasia, unilateral
• Q60.4 — Renal hypoplasia, bilateral

The remaining 58 codes are reachable through the code families above.