Genetic Diseases & Conditions - Reproductive system

Genetic changes may alter the structure or function of the reproductive system in males or females. These changes may impair fertility, or the ability to conceive a child.

Absence of vas deferens see congenital bilateral absence of vas deferens
Absent vasa see congenital bilateral absence of vas deferens
Adrenal hypoplasia congenita see X-linked adrenal hypoplasia congenita
AIS see androgen insensitivity syndrome
androgen insensitivity syndrome
AR deficiency see androgen insensitivity syndrome
Bonnevie-Ullrich Syndrome see Turner syndrome
Cancer Family Syndrome see hereditary nonpolyposis colorectal cancer
CAVD see congenital bilateral absence of vas deferens
CBAVD see congenital bilateral absence of vas deferens
CF see cystic fibrosis
COCA 1 see hereditary nonpolyposis colorectal cancer
Colon Cancer, Familial Nonpolyposis see hereditary nonpolyposis colorectal cancer
Congenital adrenal hypoplasia see X-linked adrenal hypoplasia congenita
congenital bilateral absence of vas deferens
cystic fibrosis
7-Dehydrocholesterol reductase deficiency see Smith-Lemli-Opitz syndrome
DHTR deficiency see androgen insensitivity syndrome
Dihydrotestosterone receptor deficiency see androgen insensitivity syndrome
Familial nonpolyposis colon cancer see hereditary nonpolyposis colorectal cancer
Fibrocystic Disease of Pancreas see cystic fibrosis
hereditary nonpolyposis colorectal cancer
HNPCC see hereditary nonpolyposis colorectal cancer
Klinefelter syndrome
Lynch Syndrome see hereditary nonpolyposis colorectal cancer
monosomy X see Turner syndrome
Mucoviscidosis see cystic fibrosis
RSH Syndrome see Smith-Lemli-Opitz syndrome
SLO syndrome see Smith-Lemli-Opitz syndrome
SLOS see Smith-Lemli-Opitz syndrome
Smith-Lemli-Opitz syndrome
Testicular feminisation syndrome see androgen insensitivity syndrome
TFM see androgen insensitivity syndrome
TS see Turner syndrome
Turner syndrome
Ullrich-Turner syndrome see Turner syndrome
45,X see Turner syndrome
X-linked adrenal hypoplasia congenita
47,XXY see Klinefelter syndrome
XXY syndrome see Klinefelter syndrome
XXY trisomy see Klinefelter syndrome