Other congenital malformations of male genital organs (Q55)
Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
Congenital malformations of genital organs (Q50-Q56)
Q55 Other congenital malformations of male genital organs
- Q55.0 Absence and aplasia of testis
- Q55.1 Hypoplasia of testis and scrotum
Q55.2 Other and unspecified congenital malformations 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
Q55.6 Other congenital malformations 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
Other congenital malformations of male genital organs (Q55)
Instructional Notations
Type 1 Excludes
A type 1 excludes note is a pure excludes note. It means "NOT CODED HERE!" An Excludes1 note indicates that the code excluded should never be used at the same time as the code above the Excludes1 note. An Excludes1 is used when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.
Clinical Terms
The following clinical terms provide additional context, helping users better understand the clinical background and common associations for each diagnosis listed in this section. Including related terms alongside ICD-10-CM codes supports coders, billers, and healthcare professionals in improving accuracy, enhancing documentation, and facilitating research or patient education.
Arachnodactyly
An abnormal bone development that is characterized by extra long and slender hands and fingers, such that the clenched thumb extends beyond the ulnar side of the hand. Arachnodactyly can include feet and toes. Arachnodactyly has been associated with several gene mutations and syndromes.
Priapism
A prolonged painful erection that may lasts hours and is not associated with sexual activity. It is seen in patients with SICKLE CELL ANEMIA, advanced malignancy, spinal trauma; and certain drug treatments.
WAGR Syndrome
A contiguous gene syndrome associated with hemizygous deletions of chromosome region 11p13. The condition is marked by the combination of WILMS TUMOR; ANIRIDIA; GENITOURINARY ABNORMALITIES; and INTELLECTUAL DISABILITY.