Klinefelter syndrome with karyotype 47,XXY, regular

Description

Karyotype 47 XXY; gonads: testes (hypogonadism) small and firm with decreased spermatogenesis ; phenotype male with associated congenital abnormalities (decreased virilization due to decreased testosterone production, long arms and legs, short trunk, psychosocial problems).

Index terms

Klinefelter syndrome with karyotype 47,XXY, regular
Klinefelter syndrome karyotype 47, xxy
xxy syndrome

Exclusions from above levels

http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism

Sibling codes

LD50.31 – Klinefelter syndrome, male with more than two X chromosomes
LD50.3Y – Other specified Klinefelter syndrome
LD50.3Z – Klinefelter syndrome, unspecified

Foundation entity

Klinefelter syndrome with karyotype 47,XXY, regular – http://id.who.int/icd/entity/1472503127

Part of: LD50.3: Klinefelter syndrome › LD50: Number anomalies of chromosome X › 20: Developmental anomalies