2007 ICD-9-CM Volume 1 Diagnosis Codes Home > Congenital Anomalies 740-759 >
  Congenital anomalies of genital organs- 752 is a non-specific code that cannot be used to specify a diagnosis
  Congenital anomalies of ovaries- 752.0 is a specific code that can be used to specify a diagnosis
- 752.0 contains 23 index entries
  Congenital anomalies of fallopian tubes and broad ligaments- 752.1 is a non-specific code that cannot be used to specify a diagnosis
  Unspecified congenital anomaly of fallopian tubes and broad ligaments- 752.10 is a specific code that can be used to specify a diagnosis
- 752.10 contains 6 index entries
  Embryonic cyst of fallopian tubes and broad ligaments- A cyst of the epoophoron or parovarium, a vestigial structure associated with the ovary, consisting of a more cranial group of mesonephric tubules and a corresponding portion of the mesonephric duct. (From Dorland, 27th ed)
- 752.11 is a specific code that can be used to specify a diagnosis
- 752.11 contains 21 index entries
  Other congenital anomalies of fallopian tubes and broad ligaments- 752.19 is a specific code that can be used to specify a diagnosis
- 752.19 contains 39 index entries
  Doubling of uterus- 752.2 is a specific code that can be used to specify a diagnosis
- 752.2 contains 10 index entries
  Other congenital anomalies of uterus- 752.3 is a specific code that can be used to specify a diagnosis
- 752.3 contains 47 index entries
  Congenital anomalies of cervix vagina and external female genitalia- 752.4 is a non-specific code that cannot be used to specify a diagnosis
  Unspecified congenital anomaly of cervix vagina and external female genitalia- 752.40 is a specific code that can be used to specify a diagnosis
- 752.40 contains 20 index entries
  Embryonic cyst of cervix vagina and external female genitalia- 752.41 is a specific code that can be used to specify a diagnosis
- 752.41 contains 15 index entries
  Imperforate hymen- 752.42 is a specific code that can be used to specify a diagnosis
- 752.42 contains 4 index entries
  Other congenital anomalies of cervix vagina and external female genitalia- 752.49 is a specific code that can be used to specify a diagnosis
- 752.49 contains 119 index entries
  Undescended and retractile testicle- 752.5 is a non-specific code that cannot be used to specify a diagnosis
  Undescended testis- A condition in which one or both testicles fail to move from the abdomen, where they develop before birth, into the scrotum. Undescended testicles may increase the risk for development of testicular cancer.
- A developmental defect characterized by failure of the testes to descend into the scrotum. (Dorland, 27th ed)
- site of neoplasm
- 752.51 is a specific code that can be used to specify a diagnosis
- 752.51 contains 13 index entries
  Retractile testis- 752.52 is a specific code that can be used to specify a diagnosis
- 752.52 contains 4 index entries
  Hypospadias and epispadias and other penile anomalies- 752.6 is a non-specific code that cannot be used to specify a diagnosis
  Hypospadias- A developmental anomaly in the male in which the urethra opens on the underside of the penis or on the perineum.
- 752.61 is a specific code that can be used to specify a diagnosis
- 752.61 contains 2 index entries
  Epispadias- Congenital absence of the upper wall of the urethra.
- 752.62 is a specific code that can be used to specify a diagnosis
- 752.62 contains 3 index entries
  Congenital chordee- 752.63 is a specific code that can be used to specify a diagnosis
- 752.63 contains 1 index entry
  Micropenis- 752.64 is a specific code that can be used to specify a diagnosis
- 752.64 contains 3 index entries
  Hidden penis- 752.65 is a specific code that can be used to specify a diagnosis
- 752.65 contains 3 index entries
  Other penile anomalies- 752.69 is a specific code that can be used to specify a diagnosis
- 752.69 contains 31 index entries
  Indeterminate sex and pseudohermaphroditism- A condition in which the gonads are of one sex but one or more contradictions exist in the morphologic criteria of sex. Female pseudohermaphroditism is a form in which the affected individual is a genetic and gonadal female with partial masculinization. Male pseudohermaphroditism is a form in which the affected individual is a genetic and gonadal male with incomplete masculinization. (Dorland, 27th ed)
- Originally, a state characterized by the presence of both male and female sex organs. In humans, true hermaphroditism is caused by anomalous differentiation of the gonads, with the presence of both ovarian and testicular tissue and of ambiguous morphologic criteria of sex. If only testicular tissue is present, but there are some female morphological criteria of sex, it is known as male PSEUDOHERMAPHRODITISM. If only ovarian tissue is present, but there are some male morphological criteria of sex, it is known as female PSEUDOHERMAPHRODITISM. (Dorland, 27th ed)
- 752.7 is a specific code that can be used to specify a diagnosis
- 752.7 contains 15 index entries
  Other specified anomalies of genital organs- 752.8 is a non-specific code that cannot be used to specify a diagnosis
  Scrotal transposition- 752.81 is a specific code that can be used to specify a diagnosis
- 752.81 contains 4 index entries
  Other specified anomalies of genital organs- 752.89 is a specific code that can be used to specify a diagnosis
- 752.89 contains 104 index entries
  Unspecified congenital anomaly of genital organs- 752.9 is a specific code that can be used to specify a diagnosis
- 752.9 contains 32 index entries
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