Public registry
Nodes
Browse canonical concepts by label, domain, node type, prefix and encoded class.
Current membership scope: Base domain only
| Concept | Node type | Base domain | Matched membership | Identifier |
|---|---|---|---|---|
| Gastrointestinal Diseases Diseases in any segment of the GASTROINTESTINAL TRACT from ESOPHAGUS to RECTUM. | Disorder | Pathology | Base domain | AMW:DIS:060049 |
| Gastrointestinal Hemorrhage Bleeding in any segment of the GASTROINTESTINAL TRACT from ESOPHAGUS to RECTUM. | Vascular Disorder | Pathology | Base domain | AMW:DIS:060102 |
| Gastrointestinal Mucosal Bleeding Gastrointestinal mucosal bleeding used as a ClinicalGraph target concept for pathology / pathological_process. | Pathological process | Pathology | Base domain | AMW:PROC:125011 |
| Gastrointestinal Neoplasms Tumors or cancer of the GASTROINTESTINAL TRACT, from the MOUTH to the ANAL CANAL. | Neoplastic Disorder | Pathology | Base domain | AMW:DIS:040504 |
| Gastrointestinal Stromal Tumors All tumors in the GASTROINTESTINAL TRACT arising from mesenchymal cells (MESODERM) except those of smooth muscle cells (LEIOMYOMA) or Schwann cells (… | Neoplastic Disorder | Pathology | Base domain | AMW:DIS:040165 |
| Gastroparesis Chronic delayed gastric emptying. Gastroparesis may be caused by motor dysfunction or paralysis of STOMACH muscles or may be associated with other sy… | Pathologic Condition | Pathology | Base domain | AMW:DIS:060169 |
| Gastroschisis 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 … | Congenital Disorder | Pathology | Base domain | AMW:DIS:050326 |
| GATA2 Deficiency A rare disorder of the immune system with wide-ranging effects which include GATA2 Transcription Factor dysfunction, immunodeficiency, myelodysplasti… | Congenital Disorder | Pathology | Base domain | AMW:DIS:150102 |
| Gaucher Disease An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycos… | Congenital Disorder | Pathology | Base domain | AMW:DIS:100105 |
| Genetic Diseases, Inborn Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations … | Congenital Disorder | Pathology | Base domain | AMW:DIS:160056 |
| Genetic Diseases, X-Linked 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… | Congenital Disorder | Pathology | Base domain | AMW:DIS:160059 |
| Genetic Diseases, Y-Linked 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… | Congenital Disorder | Pathology | Base domain | AMW:DIS:160062 |
| Genital Diseases Pathological processes involving the reproductive tract (GENITALIA). | Disorder | Pathology | Base domain | AMW:DIS:120272 |
| Genital Diseases, Female Pathological processes involving the female reproductive tract (GENITALIA, FEMALE). | Disorder | Pathology | Base domain | AMW:DIS:120004 |
| Genital Diseases, Male Pathological processes involving the male reproductive tract (GENITALIA, MALE). | Disorder | Pathology | Base domain | AMW:DIS:120273 |
| Genital Neoplasms, Female Tumor or cancer of the female reproductive tract (GENITALIA, FEMALE). | Neoplastic Disorder | Pathology | Base domain | AMW:DIS:040627 |
| Genital Neoplasms, Male Tumor or cancer of the MALE GENITALIA. | Neoplastic Disorder | Pathology | Base domain | AMW:DIS:040634 |
| Genomic Instability An increased tendency of the GENOME to acquire MUTATIONS when various processes involved in maintaining and replicating the genome are dysfunctional. | Pathologic Condition | Pathology | Base domain | AMW:DIS:230134 |
| Genu Valgum 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 dyspla… | Disorder | Pathology | Base domain | AMW:DIS:050094 |
| Genu Varum 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 dyspl… | Disorder | Pathology | Base domain | AMW:DIS:050095 |
| Geographic Atrophy A form of MACULAR DEGENERATION also known as dry macular degeneration marked by occurrence of a well-defined progressive lesion or atrophy in the cen… | Degenerative Disorder | Pathology | Base domain | AMW:DIS:110118 |
| Geotrichosis Infection due to the fungus Geotrichum. | Infectious Disorder | Pathology | Base domain | AMW:DIS:010270 |
| Germinoma A malignant neoplasm of the germinal tissue of the GONADS; MEDIASTINUM; or pineal region. Germinomas are uniform in appearance, consisting of large, … | Neoplastic Disorder | Pathology | Base domain | AMW:DIS:040245 |
| Gerstmann Syndrome A disorder of cognition characterized by the tetrad of finger agnosia, dysgraphia, DYSCALCULIA, and right-left disorientation. The syndrome may be de… | Syndrome | Pathology | Base domain | AMW:DIS:100508 |
| Gerstmann-Straussler-Scheinker Disease An autosomal dominant familial prion disease with a wide spectrum of clinical presentations including ATAXIA, spastic paraparesis, extrapyramidal sig… | Infectious Disorder | Pathology | Base domain | AMW:DIS:010345 |
| Gestational Trophoblastic Disease A group of diseases arising from pregnancy that are commonly associated with hyperplasia of trophoblasts (TROPHOBLAST) and markedly elevated human CH… | Neoplastic Disorder | Pathology | Base domain | AMW:DIS:040310 |
| Giant Axonal Neuropathy Rare autosomal recessive disorder of INTERMEDIATE FILAMENT PROTEINS. The disease is caused by mutations in the gene that codes gigaxonin protein. The… | Congenital Disorder | Pathology | Base domain | AMW:DIS:100385 |
| Giant Cell Arteritis A systemic autoimmune disorder that typically affects medium and large ARTERIES, usually leading to occlusive granulomatous vasculitis with transmura… | Inflammatory Disorder | Pathology | Base domain | AMW:DIS:100025 |
| Giant Cell Tumor of Bone A bone tumor composed of cellular spindle-cell stroma containing scattered multinucleated giant cells resembling osteoclasts. The tumors range from b… | Neoplastic Disorder | Pathology | Base domain | AMW:DIS:040167 |
| Giant Cell Tumor of Tendon Sheath A tumor arising in the SYNOVIAL MEMBRANE; SYNOVIAL BURSA; or TENDON sheath. It is characterized by OSTEOCLAST-like GIANT CELLS; FOAM CELLS; pigmented… | Neoplastic Disorder | Pathology | Base domain | AMW:DIS:040168 |