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 |
|---|---|---|---|---|
| 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 | Base domain | AMW:DIS:150127 |
| Granulomatous Inflammation Granulomatous inflammation used as a ClinicalGraph target concept for pathology / pathological_process. | Pathological process | Pathology | Base domain | AMW:PROC:105015 |
| 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 | Base domain | AMW:DIS:120270 |
| Granulomatous Pericardial Inflammation Granulomatous pericardial inflammation used as a ClinicalGraph target concept for pathology / pathological_process. | Pathological process | Pathology | Base domain | AMW:PROC:105011 |
| Granulosa Cell Tumor A neoplasm composed entirely of GRANULOSA CELLS, occurring mostly in the OVARY. In the adult form, it may contain some THECA CELLS. This tumor often … | Neoplastic Disorder | Pathology | Base domain | AMW:DIS:040425 |
| 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 | Base domain | 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 | Base domain | 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 | Base domain | AMW:DIS:150076 |
| Grossly Encapsulated Mass Mass surrounded by a macroscopically distinct fibrous or pseudocapsular boundary. | Pathological finding | Pathology | Base domain | AMW:FIND:180007 |
| Ground-Glass Nuclear Inclusion Homogeneous pale or ground-glass appearance of an affected nucleus due to viral material or altered chromatin. | Microscopic feature | Pathology | Base domain | AMW:FIND:230007 |
| Growth Disorders Deviations from the average values for a specific age and sex in any or all of the following: height, weight, skeletal proportions, osseous developme… | Pathologic Condition | Pathology | Base domain | AMW:DIS:230140 |
| Growth Hormone-Secreting Pituitary Adenoma A pituitary tumor that secretes GROWTH HORMONE. In humans, excess HUMAN GROWTH HORMONE leads to ACROMEGALY. | Metabolic Disorder | Pathology | Base domain | AMW:DIS:040338 |
| Guarnieri Body Eosinophilic intracytoplasmic inclusion produced by poxvirus replication. | Microscopic feature | Pathology | Base domain | AMW:FIND:230005 |
| 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 | Base domain | 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 | Base domain | 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 | Base domain | 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 | Base domain | 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 | Base domain | AMW:DIS:110050 |
| Haemonchiasis Infection with nematodes of the genus HAEMONCHUS, characterized by digestive abnormalities and anemia similar to that from hookworm infestation. | Infectious Disorder | Pathology | Base domain | AMW:DIS:010466 |
| Haemophilus Infections Infections with bacteria of the genus HAEMOPHILUS. | Infectious Disorder | Pathology | Base domain | AMW:DIS:010108 |
| Hair Diseases Diseases affecting the orderly growth and persistence of hair. | Disorder | Pathology | Base domain | AMW:DIS:170073 |
| Hajdu-Cheney Syndrome Rare, autosomal dominant syndrome characterized by ACRO-OSTEOLYSIS, generalized OSTEOPOROSIS, and skull deformations. | Syndrome | Pathology | Base domain | 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 | Base domain | AMW:DIS:230306 |
| Hallermann's Syndrome An oculomandibulofacial syndrome principally characterized by dyscephaly (usually brachycephaly), parrot nose, mandibular hypoplasia, proportionate n… | Syndrome | Pathology | Base domain | 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 | Base domain | 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 | Base domain | 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 | Base domain | 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 | Base domain | 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 | Base domain | AMW:DIS:050160 |
| Hamartoma A focal malformation resembling a neoplasm, composed of an overgrowth of mature cells and tissues that normally occur in the affected area. | Neoplastic Disorder | Pathology | Base domain | AMW:DIS:040041 |