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Items: 1 to 20 of 22

1.

Y chromosome deletions

MedGen UID:
419727
Concept ID:
C2931163
Disease or Syndrome
2.

Subfertility, Male

MedGen UID:
452752
Concept ID:
C0848676
Sign or Symptom
3.

Subfertility, Female

MedGen UID:
452445
Concept ID:
C0341869
Disease or Syndrome
4.

Male sterility

MedGen UID:
182408
Concept ID:
C0917731
Finding
5.

Female sterility

MedGen UID:
181472
Concept ID:
C0917730
Finding
6.

Azoospermia

A condition of having no sperm present in the ejaculate (SEMEN). [from MeSH]

MedGen UID:
2150
Concept ID:
C0004509
Disease or Syndrome
7.

Azoospermia

Absence of any measurable level of sperm in his semen. [from HPO]

MedGen UID:
504308
Concept ID:
CN000028
Finding
8.

Reproductive Sterility

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

MedGen UID:
882191
Concept ID:
C4074771
Pathologic Function
9.

Subfertility

MedGen UID:
452706
Concept ID:
C0729353
Disease or Syndrome
10.

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
11.

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
12.

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
13.

Biosynthesis, Peptide

The production of PEPTIDES or PROTEINS by the constituents of a living organism. The biosynthesis of proteins on RIBOSOMES following an RNA template is termed translation (TRANSLATION, GENETIC). There are other, non-ribosomal peptide biosynthesis (PEPTIDE BIOSYNTHESIS, NUCLEIC ACID-INDEPENDENT) mechanisms carried out by PEPTIDE SYNTHASES and PEPTIDYLTRANSFERASES. Further modifications of peptide chains yield functional peptide and protein molecules. [from MeSH]

MedGen UID:
272130
Concept ID:
C1327133
Molecular Function
14.

Protein Modification, Translational

Any of the enzymatically catalyzed modifications of the individual AMINO ACIDS of PROTEINS, and enzymatic cleavage or crosslinking of peptide chains that occur pre-translationally (on the amino acid component of AMINO ACYL TRNA), co-translationally (during the process of GENETIC TRANSLATION), or after translation is completed (POST-TRANSLATIONAL PROTEIN PROCESSING). [from MeSH]

MedGen UID:
260537
Concept ID:
C1449566
Molecular Function
15.

Genetic translation

Protein synthesis is the group of processes that are involved in generation of mature protein molecules. Although protein synthesis may involve translation alone in many cases, in others, it involves also protein folding, integration of prosthetic groups, glycosylation, methylation, phosphorylation, lipidation and any other process that may be involved in maturation of the polypeptide to the biologically active form. [from NCI]

MedGen UID:
108933
Concept ID:
C0597295
Molecular Function
16.

Post-Translational Modification

The enzymatic processing of a polypeptide chain after translation from messenger RNA and after peptide bond formation has occurred. Examples include glycosylation, acylation, limited proteolysis, phosphorylation, isoprenylation.(On-line Medical Dictionary) [from NCI]

MedGen UID:
46159
Concept ID:
C0033666
Molecular Function
17.

Infertility

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

MedGen UID:
43876
Concept ID:
C0021359
Finding; Pathologic Function
18.

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
19.

Sterility, Postpartum

MedGen UID:
11592
Concept ID:
C0038279
Pathologic Function
20.

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
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