Certain infectious and parasitic diseases
Certain infectious and parasitic diseases Certain infectious and parasitic diseases
Q54.0 Hypospadias, balanic Hypospadias: · coronal · glandular 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 Other congenital malformations of male genital organs Excludes: congenital hydrocele ( P83.5 ) hypospadias ( Q54.- ) Q55.0 Absence and aplasia of testis Monorchism Q55.1 Hypoplasia of testis and scrotum Fusion of testes Q55.2 Other congenital malformations of testis and scrotum Congenital malformation of testis or scrotum NOS Polyorchism Retractile testis Testis migrans Q55.3 Atresia of vas deferens Q55.4 Other congenital malformations of vas deferens, epididymis, seminal vesicles and prostate Absence or aplasia of: · prostate · spermatic cord Congenital malformation of vas deferens, epididymis, seminal vesicles or prostate NOS Q55.5 Congenital absence and aplasia of penis Q55.6 Other congenital malformations of penis Congenital malformation of penis NOS Curvature of penis (lateral) Hypoplasia of penis Q55.8 Other specified congenital malformations of male genital organs Q55.9 Congenital malformation of male genital organ, unspecified Congenital: · anomaly · deformity } NOS of male genital organ 562 WHO’s ICD-10
Q56 Indeterminate sex and pseudohermaphroditism Excludes: pseudohermaphroditism: · female, with adrenocortical disorder ( E25.- ) · male, with androgen resistance ( E34.5 ) · with specified chromosomal anomaly ( Q96-Q99 ) Q56.0 Hermaphroditism, not elsewhere classified Ovotestis Q56.1 Male pseudohermaphroditism, not elsewhere classified Male pseudohermaphroditism NOS Q56.2 Female pseudohermaphroditism, not elsewhere classified Female pseudohermaphroditism NOS Q56.3 Pseudohermaphroditism, unspecified Q56.4 Indeterminate sex, unspecified Ambiguous genitalia Congenital malformations of the urinary system (Q60-Q64) Q60 Renal agenesis and other reduction defects of kidney Includes: atrophy of kidney: · congenital · infantile congenital absence of kidney 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 Q60.5 Renal hypoplasia, unspecified Q60.6 Potter's syndrome Q61 Cystic kidney disease Excludes: acquired cyst of kidney ( N28.1 ) Potter's syndrome ( Q60.6 ) Q61.0 Congenital single renal cyst Cyst of kidney (congenital)(single) Q61.1 Polycystic kidney, autosomal recessive Polycystic kidney, infantile type Q61.2 Polycystic kidney, autosomal dominant Polycystic kidney, adult type Version for 2007 563
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Q56 Indeterminate sex <strong>and</strong> pseudohermaphroditism<br />
Excludes: pseudohermaphroditism:<br />
· female, with adrenocortical disorder ( E25.- )<br />
· male, with <strong>and</strong>rogen resistance ( E34.5 )<br />
· with specified chromosomal anomaly ( Q96-Q99 )<br />
Q56.0 Hermaphroditism, not elsewhere classified<br />
Ovotestis<br />
Q56.1 Male pseudohermaphroditism, not elsewhere classified<br />
Male pseudohermaphroditism NOS<br />
Q56.2 Female pseudohermaphroditism, not elsewhere classified<br />
Female pseudohermaphroditism NOS<br />
Q56.3 Pseudohermaphroditism, unspecified<br />
Q56.4 Indeterminate sex, unspecified<br />
Ambiguous genitalia<br />
Congenital malformations of the urinary system<br />
(Q60-Q64)<br />
Q60 Renal agenesis <strong>and</strong> other reduction defects of kidney<br />
Includes: atrophy of kidney:<br />
· congenital<br />
· infantile<br />
congenital absence of kidney<br />
Q60.0 Renal agenesis, unilateral<br />
Q60.1 Renal agenesis, bilateral<br />
Q60.2 Renal agenesis, unspecified<br />
Q60.3 Renal hypoplasia, unilateral<br />
Q60.4 Renal hypoplasia, bilateral<br />
Q60.5 Renal hypoplasia, unspecified<br />
Q60.6 Potter's syndrome<br />
Q61 Cystic kidney disease<br />
Excludes: acquired cyst of kidney ( N28.1 )<br />
Potter's syndrome ( Q60.6 )<br />
Q61.0 Congenital single renal cyst<br />
Cyst of kidney (congenital)(single)<br />
Q61.1 Polycystic kidney, autosomal recessive<br />
Polycystic kidney, infantile type<br />
Q61.2 Polycystic kidney, autosomal dominant<br />
Polycystic kidney, adult type<br />
Version for 2007 563
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