Public registry
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Browse canonical concepts by label, domain, node type, prefix and encoded class.
Current membership scope: Domain and all descendants
| Concept | Node type | Base domain | Matched membership | Identifier |
|---|---|---|---|---|
| Graft Occlusion, Vascular Obstruction of flow in biological or prosthetic vascular grafts. | Vascular Disorder | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:230201 |
| Graft vs Host Disease The clinical entity characterized by anorexia, diarrhea, loss of hair, leukopenia, thrombocytopenia, growth retardation, and eventual death brought a… | Immune Disorder | Pathology | Immune System [curated_secondary] | AMW:DIS:200006 |
| Granuloma A relatively small nodular inflammatory lesion containing grouped mononuclear phagocytes, caused by infectious and noninfectious agents. | Pathologic Condition | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150156 |
| Granuloma Annulare Benign granulomatous disease of unknown etiology characterized by a ring of localized or disseminated papules or nodules on the skin and palisading h… | Pathologic Condition | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170008 |
| Granuloma, Giant Cell A non-neoplastic inflammatory lesion, usually of the jaw or gingiva, containing large, multinucleated cells. It includes reparative giant cell granul… | Pathologic Condition | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050172 |
| Granuloma, Laryngeal A tumor-like nodule or mass of inflammatory granulation tissue projecting into the lumen of the LARYNX. | Pathologic Condition | Pathology | Respiratory System [curated_secondary] | AMW:DIS:080022 |
| Granuloma, Lethal Midline A condition that is characterized by inflammation, ulceration, and perforation of the nose and the PALATE with progressive destruction of midline fac… | Disorder | Pathology | Respiratory System [curated_secondary] | AMW:DIS:080096 |
| Granuloma, Respiratory Tract Granulomatous disorders affecting one or more sites in the respiratory tract. | Pathologic Condition | Pathology | Respiratory System [curated_secondary] | AMW:DIS:080021 |
| Granulomatosis with Polyangiitis A multisystemic disease of a complex genetic background. It is characterized by inflammation of the blood vessels (VASCULITIS) leading to damage in a… | Inflammatory Disorder | Pathology | Respiratory System [curated_secondary] | AMW:DIS:080067 |
| Granulomatous Disease, Chronic A defect of leukocyte function in which phagocytic cells ingest but fail to digest bacteria, resulting in recurring bacterial infections with granulo… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150127 |
| Granulomatous Mastitis A rare, benign, inflammatory breast disease occurring in premenopausal women shortly after a recent pregnancy. The origin is unknown but it is common… | Inflammatory Disorder | Pathology | Reproductive System [curated_secondary] | AMW:DIS:120270 |
| Graves Disease A common form of hyperthyroidism with a diffuse hyperplastic GOITER. It is an autoimmune disorder that produces antibodies against the THYROID STIMUL… | Metabolic Disorder | Pathology | Visual System [curated_secondary] | AMW:DIS:110096 |
| Graves Ophthalmopathy An autoimmune disorder of the EYE, occurring in patients with Graves disease. Subtypes include congestive (inflammation of the orbital connective tis… | Congenital Disorder | Pathology | Visual System [curated_secondary] | AMW:DIS:110049 |
| Gray Platelet Syndrome A rare, inherited platelet disorder characterized by a selective deficiency in the number and contents of platelet alpha-granules. It is associated w… | Syndrome | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150076 |
| Guillain-Barre Syndrome An acute inflammatory autoimmune neuritis caused by T cell- mediated cellular immune response directed towards peripheral myelin. Demyelination occur… | Immune Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100019 |
| Guttate Psoriasis A skin condition, typically emerges suddenly and frequently occurs after an infection such as STREPTOCOCCAL INFECTION. While prevalent among children… | Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170133 |
| Gynatresia Absence of a normal opening in the lumen of the female genital tract, from the FALLOPIAN TUBES to the VAGINA. This anomaly may be congenital or acqui… | Pathologic Condition | Pathology | Reproductive System [curated_secondary] | AMW:DIS:120019 |
| Gynecomastia Enlargement of the BREAST in the males, caused by an excess of ESTROGENS. Physiological gynecomastia is normally observed in NEWBORNS; ADOLESCENT; an… | Disorder | Pathology | Reproductive System [curated_secondary] | AMW:DIS:170035 |
| Gyrate Atrophy Progressive, autosomal recessive, diffuse atrophy of the choroid, pigment epithelium, and sensory retina that begins in childhood. | Degenerative Disorder | Pathology | Visual System [curated_secondary] | AMW:DIS:110050 |
| Hair Diseases Diseases affecting the orderly growth and persistence of hair. | Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170073 |
| Hajdu-Cheney Syndrome Rare, autosomal dominant syndrome characterized by ACRO-OSTEOLYSIS, generalized OSTEOPOROSIS, and skull deformations. | Syndrome | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050005 |
| Halitosis An offensive, foul breath odor resulting from a variety of causes such as poor oral hygiene, dental or oral infections, or the ingestion of certain f… | Pathologic Condition | Pathology | Digestive System [curated_secondary] | AMW:DIS:230306 |
| Hallermann's Syndrome An oculomandibulofacial syndrome principally characterized by dyscephaly (usually brachycephaly), parrot nose, mandibular hypoplasia, proportionate n… | Syndrome | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050017 |
| Hallucinations Subjectively experienced sensations in the absence of an appropriate stimulus, but which are regarded by the individual as real. They may be of organ… | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100511 |
| Hallux Limitus A bony proliferation and articular degeneration of the first METATARSOPHALANGEAL JOINT that is characterized by pain and a progressive decrease in th… | Traumatic Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050151 |
| Hallux Rigidus A condition caused by degenerative arthritis (see OSTEOARTHRITIS) of the METATARSOPHALANGEAL JOINT of the great toe and characterized by pain and lim… | Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050152 |
| Hallux Valgus Lateral displacement of the great toe (HALLUX), producing deformity of the first METATARSOPHALANGEAL JOINT with callous, bursa, or BUNION formation o… | Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050159 |
| Hallux Varus Displacement of the great toe (HALLUX) towards the midline or away from the other TOES. It can be congenital or acquired. | Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050160 |
| Hamman-Rich Syndrome Acute idiopathic interstitial pneumonitis characterized by diffuse PULMONARY ALVEOLI damage with uniform edematous connective tissue proliferation. I… | Syndrome | Pathology | Respiratory System [curated_secondary] | AMW:DIS:080063 |
| Hammer Toe Syndrome A condition characterized by a series of interrelated digital symptoms and joint changes of the lesser digits and METATARSOPHALANGEAL JOINTS of the F… | Syndrome | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050161 |