All terms in MeSH

Label Id Description
Adoxaceae D031003 [A plant genus of the family Adoxaceae. , A plant family of the order Dipsacales, subclass Asteridae, class Magnoliopsida. Members of this family are sometimes classified in CAPRIFOLIACEAE. ]
3-Iodobenzylguanidine D02.455.426.559.389.454.300
Horse Diseases C22.488
Lavandula B01.650.940.800.575.912.250.583.520.428
Tattooing E02.218.085.840
Body Modification, Non-Therapeutic E02.218.085
Golgi-Mazzoni Corpuscles D006057 [Thin capsules enveloping end nerve fibrils in the subcutaneous tissue of fingers. ]
Coated Materials, Biocompatible J01.637.051.130.420
Gonadal Disorders D006058 [Pathological processes of the OVARIES or the TESTES. ]
Entomoplasmataceae D045622 [A genus of non-sterol-requiring insect and plant TENERICUTES in the family Entomoplasmataceae. , A family of gram-negative, nonhelical, arthropod-associated bacteria in the order Entomoplasmatales. It is comprised of two genera: Entomoplasma and Mesoplasma. , A genus of TENERICUTES in the family Entomoplasmataceae. ]
Gonadal Dysgenesis D006059 [A number of syndromes with defective gonadal developments such as streak GONADS and dysgenetic testes or ovaries. The spectrum of gonadal and sexual abnormalities is reflected in their varied sex chromosome (SEX CHROMOSOMES) constitution as shown by the karyotypes of 45,X monosomy (TURNER SYNDROME); 46,XX (GONADAL DYSGENESIS, 46XX); 46,XY (GONADAL DYSGENESIS, 46,XY); and sex chromosome MOSAICISM; (GONADAL DYSGENESIS, MIXED). Their phenotypes range from female, through ambiguous, to male. This concept includes gonadal agenesis. , The complete failure of gonadal development. ]
Mycoplasma capricolum D045623 [A genus in the family ENTOMOPLASMATACEAE, order Entomoplasmatales. It is pathogenic to GOATS, causing caprine pleuropneumonia (PLEUROPNEUMONIA, CONTAGIOUS). ]
Gonadotropins, Equine D006064 [Gonadotropins secreted by the pituitary or the placenta in horses. This term generally refers to the gonadotropins found in the pregnant mare serum, a rich source of equine CHORIONIC GONADOTROPIN; LUTEINIZING HORMONE; and FOLLICLE STIMULATING HORMONE. Unlike that in humans, the equine LUTEINIZING HORMONE, BETA SUBUNIT is identical to the equine choronic gonadotropin, beta. Equine gonadotropins prepared from pregnant mare serum are used in reproductive studies. ]
Gonadotropins, Pituitary D006065 [Hormones secreted by the adenohypophysis (PITUITARY GLAND, ANTERIOR) that stimulate gonadal functions in both males and females. They include FOLLICLE STIMULATING HORMONE that stimulates germ cell maturation (OOGENESIS; SPERMATOGENESIS), and LUTEINIZING HORMONE that stimulates the production of sex steroids (ESTROGENS; PROGESTERONE; ANDROGENS). ]
Gonads D006066 [The gamete-producing glands, OVARY or TESTIS. ]
Cell Degranulation G04.468.160
Gonanes D006067 [Steroids containing the fundamental tetracyclic unit with no methyl groups at C-10 and C-13 and with no side chain at C-17. The concept includes both saturated and unsaturated derivatives. ]
Gonadal Dysgenesis, Mixed D006060 [A type of defective gonadal development in patients with a wide spectrum of chromosomal mosaic variants. Their karyotypes are of partial sex chromosome monosomy resulting from an absence or an abnormal second sex chromosome (X or Y). Karyotypes include 45,X/46,XX; 45,X/46,XX/47,XXX; 46,XXp-; 45,X/46,XY; 45,X/47,XYY; 46,XYpi; etc. The spectrum of phenotypes may range from phenotypic female to phenotypic male including variations in gonads and internal and external genitalia, depending on the ratio in each gonad of 45,X primordial germ cells to those with normal 46,XX or 46,XY constitution. ]
Gonadal Dysgenesis, 46,XY D006061 [Defects in the SEX DETERMINATION PROCESS in 46, XY individuals that result in abnormal gonadal development and deficiencies in TESTOSTERONE and subsequently ANTIMULLERIAN HORMONE or other factors required for normal male sex development. This leads to the development of female phenotypes (male to female sex reversal), normal to tall stature, and bilateral streak or dysgenic gonads which are susceptible to GONADAL TISSUE NEOPLASMS. An XY gonadal dysgenesis is associated with structural abnormalities on the Y CHROMOSOME, a mutation in the GENE, SRY, or a mutation in other autosomal genes that are involved in sex determination. ]
Myocardial Reperfusion Injury C23.550.767.877.500