Disorder of Sex Development, 46,XY [poruchy sexuálního vývoje s karyotypem 46, XY]

topical
8
Terms

46, XY DSD
46,XY DSD
mužský pseudohermafroditismus

 

46, XY Disorders of Sex Development
46, XY DSD
46,XY Disorders of Sex Development
46,XY DSD
46,XY Gonadal Dysgenesis, Complete or Partial, With or Without Adrenal Failure
46,XY Sex Reversal 3
46,XY Sex Reversal, Partial or Complete, NR5A1-Related
Male Pseudohermaphroditism
Sex Reversal, XY, With Or Without Adrenal Failure

Persistent link   https://www.medvik.cz/link/D058490
Definition

Congenital conditions in individuals with a male karyotype, in which the development of the gonadal or anatomical sex is atypical.

DUI
D058490 MeSH Browser
CUI
M0542825
History note
2019(2011); for MALE PSEUDOHERMAPHRODITISM use DISORDERS OF SEX DEVELOPMENT 2006-2010
Public note
2019; for MALE PSEUDOHERMAPHRODITISM see PSEUDOHERMAPHRODITISM 2006-2010

C Diseases
C12.050.351.875 Urogenital Abnormalities 146
C12.050.351.875.253 Disorders of Sex Development 232
C12.050.351.875.253.064 46, XX Disorders of Sex Development 20
C12.050.351.875.253.090 Adrenogenital Syndrome 50
C12.050.351.875.253.096 Disorder of Sex Development, 46,XY 8
C12.050.351.875.253.096.500 Androgen-Insensitivity Syndrome 56
C12.050.351.875.253.096.562 Denys-Drash Syndrome 2
C12.050.351.875.253.096.624 Frasier Syndrome
C12.050.351.875.253.096.687 Gonadal Dysgenesis, 46,XY 22
C12.050.351.875.253.096.750 Kallmann Syndrome 10
C12.050.351.875.253.096.875 WAGR Syndrome 3
C12.050.351.875.253.309 Gonadal Dysgenesis 59
C12.200.706.316 Disorders of Sex Development 232
C12.200.706.316.090 Adrenogenital Syndrome 50
C12.200.706.316.096.500 Androgen-Insensitivity Syndrome 56
C12.200.706.316.096.562 Denys-Drash Syndrome 2
C12.200.706.316.096.624 Frasier Syndrome
C12.200.706.316.096.687 Gonadal Dysgenesis, 46,XY 22
C12.200.706.316.096.750 Kallmann Syndrome 10
C12.200.706.316.096.875 WAGR Syndrome 3
C12.200.706.316.309 Gonadal Dysgenesis 59
C12.800.316.090 Adrenogenital Syndrome 50
C12.800.316.096.500 Androgen-Insensitivity Syndrome 56
C12.800.316.096.562 Denys-Drash Syndrome 2
C12.800.316.096.624 Frasier Syndrome
C12.800.316.096.687 Gonadal Dysgenesis, 46,XY 22
C12.800.316.096.750 Kallmann Syndrome 10
C12.800.316.096.875 WAGR Syndrome 3
C12.800.316.309 Gonadal Dysgenesis 59
C16.131.939.316 Disorders of Sex Development 232
C16.131.939.316.096.500 Androgen-Insensitivity Syndrome 56
C16.131.939.316.096.562 Denys-Drash Syndrome 2
C16.131.939.316.096.624 Frasier Syndrome
C16.131.939.316.096.687 Gonadal Dysgenesis, 46,XY 22
C16.131.939.316.096.750 Kallmann Syndrome 10
C16.131.939.316.096.875 WAGR Syndrome 3
C16.131.939.316.129 Adrenogenital Syndrome 50
C16.131.939.316.309 Gonadal Dysgenesis 59
C19.391.119.090 Adrenogenital Syndrome 50
C19.391.119.096.500 Androgen-Insensitivity Syndrome 56
C19.391.119.096.562 Denys-Drash Syndrome 2
C19.391.119.096.624 Frasier Syndrome
C19.391.119.096.687 Gonadal Dysgenesis, 46,XY 22
C19.391.119.096.750 Kallmann Syndrome 10
C19.391.119.096.875 WAGR Syndrome 3
C19.391.119.309 Gonadal Dysgenesis 59

17-Hydroxysteroid Dehydrogenase Deficiency Disease MeSH Browser

46,Xy True Hermaphroditism, Sry-Related Disease MeSH Browser

Leydig Cell Hypoplasia Disease MeSH Browser

Lipoid congenital adrenal hyperplasia Disease MeSH Browser

Male pseudohermaphroditism due to defective LH molecule Disease MeSH Browser

Male pseudohermaphroditism-mental retardation syndrome, Verloes type Disease MeSH Browser

Nivelon Nivelon Mabille syndrome Disease MeSH Browser

Persistent Mullerian duct syndrome Disease MeSH Browser

Pseudovaginal Perineoscrotal Hypospadias Disease MeSH Browser

Urioste Martinez-Frias syndrome Disease MeSH Browser