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Items: 1 to 20 of 24

1.

Subfertility, Male

MedGen UID:
452752
Concept ID:
C0848676
Sign or Symptom
2.

Male sterility

MedGen UID:
182408
Concept ID:
C0917731
Finding
3.

Infertility

A reduced or absent capacity to reproduce. [from MeSH]

MedGen UID:
43876
Concept ID:
C0021359
Finding; Pathologic Function
4.

Reproductive Sterility

Complete inability to conceive or induce conception. [from MeSH]

MedGen UID:
882191
Concept ID:
C4074771
Pathologic Function
5.

Subfertility, Female

MedGen UID:
452445
Concept ID:
C0341869
Disease or Syndrome
6.

Female sterility

MedGen UID:
181472
Concept ID:
C0917730
Finding
7.

Ovarian failure

The inability of the ovaries to function. [from NCI]

MedGen UID:
677092
Concept ID:
C0747102
Disease or Syndrome
8.

Infertility

MedGen UID:
504598
Concept ID:
CN000737
Finding
9.

Invasion

The movement of one cell type into an area normally occupied by a different cell type. [from NCI]

MedGen UID:
397081
Concept ID:
C2699153
Pathologic Function
10.

Premature ovarian failure

Premature ovarian failure is clearly a heterogeneous disorder. The terms 'hypergonadotropic ovarian failure' and 'hypergonadotropic ovarian dysgenesis' (see ODG1, 233300) have been used to indicate a group of disorders in which amenorrhea associated with elevated levels of serum gonadotropins occurs long before the age of 40 years (Coulam, 1982). Cytogenetic studies of X-chromosome aberrations have suggested that it is mainly the long arm of the X chromosome that is involved in defects of ovulation (Bione et al., 1998). Genetic Heterogeneity of Premature Ovarian Failure Mutations in genes identified within a region defined as POF2 (Xq13.3-q21.1) have been found to cause other forms of POF: POF2A (300511) by mutation in the DIAPH2 gene (300108) and POF2B (300604) by mutation in the POF1B gene (300603). See also POF3 (608996), caused by mutation in the FOXL2 gene (605597) on chromosome 3q22; POF4 (see 300510), caused by mutation in the BMP15 gene (300247) on chromosome Xp11; POF5 (611548), caused by mutation in the NOBOX gene (610934) on chromosome 7q35; POF6 (612310), caused by mutation in the FIGLA gene (608697) on chromosome 2p13; POF7 (612964), caused by mutation in the NR5A1 gene (184757) on chromosome 9q33; POF8 (615723), caused by mutation in the STAG3 gene (608489) on chromosome 7q22; POF9 (615724), caused by mutation in the HFM1 gene (615684) on chromosome 1p22; POF10 (612885), caused by mutation in the MCM8 gene (608187) on chromosome 20p12; POF11 (616946), caused by mutation in the ERCC6 gene (609413) on chromosome 10q11; POF12 (616947), caused by mutation in the SYCE1 gene (611486) on chromosome 10q26; and POF13 (617442), caused by mutation in the MSH5 gene (603382) on chromosome 6p22. [from GTR]

MedGen UID:
38820
Concept ID:
C0085215
Disease or Syndrome
11.

Premature ovarian failure

Cessation of menstruation before the age of 40. Symptoms include hot flashes, night sweats, mood swings, and decreased sex drive. [from NCI]

MedGen UID:
9963
Concept ID:
C0025322
Disease or Syndrome
12.

Subfertility

MedGen UID:
452706
Concept ID:
C0729353
Disease or Syndrome
13.

Male Urogenital Diseases

Pathological processes of the male URINARY TRACT and the reproductive system (GENITALIA, MALE). [from MeSH]

MedGen UID:
318601
Concept ID:
C1720894
Disease or Syndrome
14.

Female Urogenital Diseases

Pathological processes of the female URINARY TRACT and the reproductive system (GENITALIA, FEMALE). [from MeSH]

MedGen UID:
318599
Concept ID:
C1720887
Disease or Syndrome
15.

Female Urogenital Diseases and Pregnancy Complications

Pathological processes of the female URINARY TRACT, the reproductive system (GENITALIA, FEMALE), and disorders related to PREGNANCY. [from MeSH]

MedGen UID:
318565
Concept ID:
C1720765
Disease or Syndrome
16.

Disorder of male genital organ

Pathological processes involving the male reproductive tract (GENITALIA, MALE). [from MeSH]

MedGen UID:
42195
Concept ID:
C0017412
Disease or Syndrome
17.

Sterility, Postpartum

MedGen UID:
11592
Concept ID:
C0038279
Pathologic Function
18.

Disorder of female genital system

Pathological processes involving the female reproductive tract (GENITALIA, FEMALE). [from MeSH]

MedGen UID:
9003
Concept ID:
C0017411
Disease or Syndrome
19.

Male infertility

The inability of the male to effect FERTILIZATION of an OVUM after a specified period of unprotected intercourse. Male sterility is permanent infertility. [from MeSH]

MedGen UID:
5796
Concept ID:
C0021364
Disease or Syndrome
20.

Female infertility

Diminished or absent ability of a female to achieve conception. [from MeSH]

MedGen UID:
5795
Concept ID:
C0021361
Pathologic Function
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