Terminology Service < Semantic Lookup Platform

All individuals in MESHD

Label	Id	Description
Gastrointestinal Hemorrhage	D006471	[Bleeding in any segment of the GASTROINTESTINAL TRACT from ESOPHAGUS to RECTUM., The passage of bright red blood from the rectum. The blood may or may not be mixed with formed stool in the form of blood, blood clots, bloody stool or diarrhea.]
Gastrointestinal Neoplasms	D005770	[Tumors or cancer of the GASTROINTESTINAL TRACT, from the MOUTH to the ANAL CANAL.]
Gastrointestinal Stromal Tumors	D046152	[All tumors in the GASTROINTESTINAL TRACT arising from mesenchymal cells (MESODERM) except those of smooth muscle cells (LEIOMYOMA) or Schwann cells (SCHWANNOMA).]
Gastroparesis	D018589	[Chronic delayed gastric emptying. Gastroparesis may be caused by motor dysfunction or paralysis of STOMACH muscles or may be associated with other systemic diseases such as DIABETES MELLITUS.]
Gastroschisis	D020139	[A congenital defect with major fissure in the ABDOMINAL WALL lateral to, but not at, the UMBILICUS. This results in the extrusion of VISCERA. Unlike OMPHALOCELE, herniated structures in gastroschisis are not covered by a sac or PERITONEUM.]
Gaucher Disease	D005776	[This type usually shows severe neurological effect in the first year of life., An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement., This type shows moderate to severe neurological effect in childhood., This type afflicts both children and adults who show no neurological effect. It is more prevalent in people of Ashkenazi Jewish ancestry.]
Genetic Diseases, Inborn	D030342	[Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero., Diseases caused by genetic mutations that are inherited from a parent's genome.]
Genetic Diseases, X-Linked	D040181	[Genetic diseases that are linked to gene mutations on the X CHROMOSOME in humans (X CHROMOSOME, HUMAN) or the X CHROMOSOME in other species. Included here are animal models of human X-linked diseases.]
Genetic Diseases, Y-Linked	D050174	[Genetic diseases that are linked to mutant ALLELES on the Y CHROMOSOME in humans (Y CHROMOSOME, HUMAN) or the Y chromosome in other species. Included here are animal models of human Y-linked diseases.]
Genetic Predisposition to Disease	D020022	[A latent susceptibility to disease at the genetic level, which may be activated under certain conditions.]
Genital Diseases, Female	D005831	[Pathological processes involving the female reproductive tract (GENITALIA, FEMALE).]
Genital Diseases, Male	D005832	[Pathological processes involving the male reproductive tract (GENITALIA, MALE).]
Genital Neoplasms, Female	D005833	[Tumor or cancer of the female reproductive tract (GENITALIA, FEMALE).]
Genital Neoplasms, Male	D005834	[Tumor or cancer of the MALE GENITALIA.]
Genomic Instability	D042822	[An increased tendency of the GENOME to acquire MUTATIONS when various processes involved in maintaining and replicating the genome are dysfunctional.]
Genu Valgum	D056304	[An inward slant of the thigh in which the knees are close together and the ankles far apart. Genu valgum can develop due to skeletal and joint dysplasias (e.g., OSTEOARTHRITIS; HURLER SYNDROME); and malnutrition (e.g., RICKETS; FLUORIDE POISONING).]
Genu Varum	D056305	[An outward slant of the thigh in which the knees are wide apart and the ankles close together. Genu varum can develop due to skeletal and joint dysplasia (e.g., OSTEOARTHRITIS; Blount's disease); and malnutrition (e.g., RICKETS; FLUORIDE POISONING).]
Geographic Atrophy	D057092	[A form of MACULAR DEGENERATION also known as dry macular degeneration marked by occurrence of a well-defined progressive lesion or atrophy in the central part of the RETINA called the MACULA LUTEA. It is distinguishable from WET MACULAR DEGENERATION in that the latter involves neovascular exudates.]
Geotrichosis	D005847	[Infection due to the fungus Geotrichum.]
Germinoma	D018237	[A malignant neoplasm of the germinal tissue of the GONADS; MEDIASTINUM; or pineal region. Germinomas are uniform in appearance, consisting of large, round cells with vesicular nuclei and clear or finely granular eosinophilic-staining cytoplasm. (Stedman, 265th ed; from DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, pp1642-3)]