Public registry
Nodes
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 |
|---|---|---|---|---|
| Barth Syndrome Rare congenital X-linked disorder of lipid metabolism. Barth syndrome is transmitted in an X-linked recessive pattern. The syndrome is characterized … | Syndrome | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140007 |
| Bartter Syndrome A group of disorders caused by defective salt reabsorption in the ascending LOOP OF HENLE. It is characterized by severe salt-wasting, HYPOKALEMIA; H… | Syndrome | Pathology | Renal and Urinary System [curated_secondary] | AMW:DIS:120145 |
| Basal Ganglia Cerebrovascular Disease A pathological condition caused by impaired blood flow in the basal regions of cerebral hemispheres (BASAL GANGLIA), such as INFARCTION; HEMORRHAGE; … | Vascular Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100053 |
| Basal Ganglia Diseases Diseases of the BASAL GANGLIA including the PUTAMEN; GLOBUS PALLIDUS; claustrum; AMYGDALA; and CAUDATE NUCLEUS. DYSKINESIAS (most notably involuntary… | Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100052 |
| Basal Ganglia Hemorrhage Bleeding within the subcortical regions of cerebral hemispheres (BASAL GANGLIA). It is often associated with HYPERTENSION or ARTERIOVENOUS MALFORMATI… | Vascular Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100054 |
| Bernard-Soulier Syndrome A familial coagulation disorder characterized by a prolonged bleeding time, unusually large platelets, and impaired prothrombin consumption. | Syndrome | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150045 |
| Berylliosis A form of pneumoconiosis caused by inhaled rare metal BERYLLIUM or its soluble salts which are used in a wide variety of industry including alloys, c… | Exposure Related Disorder | Pathology | Respiratory System [curated_secondary] | AMW:DIS:080057 |
| beta-Thalassemia A disorder characterized by reduced synthesis of the beta chains of hemoglobin. There is retardation of hemoglobin A synthesis in the heterozygous fo… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150024 |
| Bicornuate Uterus A congenital uterine anomaly in which the UTERUS is divided into two uterine horns with a significant cleft at the uterine fundus due to partial fusi… | Disorder | Pathology | Reproductive System [curated_secondary] | AMW:DIS:120031 |
| Bicuspid Aortic Valve Disease Congenital heart valve defects where the AORTIC VALVE has two instead of normal three cusps. It is often associated with AORTIC REGURGITATION and AOR… | Congenital Disorder | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140008 |
| Bile Duct Diseases Diseases in any part of the ductal system of the BILIARY TRACT from the smallest BILE CANALICULI to the largest COMMON BILE DUCT. | Disorder | Pathology | Digestive System [curated_secondary] | AMW:DIS:060003 |
| Bile Reflux Retrograde bile flow. Reflux of bile can be from the duodenum to the stomach (DUODENOGASTRIC REFLUX); to the esophagus (GASTROESOPHAGEAL REFLUX); or … | Disorder | Pathology | Digestive System [curated_secondary] | AMW:DIS:060019 |
| Biliary Atresia Progressive destruction or the absence of all or part of the extrahepatic BILE DUCTS, resulting in the complete obstruction of BILE flow. Usually, bi… | Pathologic Condition | Pathology | Digestive System [curated_secondary] | AMW:DIS:060004 |
| Biliary Colic Biliary colic used as a ClinicalGraph target concept for pathology / disease. | Disorder | Pathology | Digestive System [curated_secondary] | AMW:DIS:060243 |
| Biliary Dyskinesia A motility disorder characterized by biliary COLIC, absence of GALLSTONES, and an abnormal GALLBLADDER ejection fraction. It is caused by gallbladder… | Disorder | Pathology | Digestive System [curated_secondary] | AMW:DIS:060015 |
| Biliary Fistula Abnormal passage in any organ of the biliary tract or between biliary organs and other organs. | Pathologic Condition | Pathology | Digestive System [curated_secondary] | AMW:DIS:060041 |
| Biliary Tract Diseases Diseases in any part of the BILIARY TRACT including the BILE DUCTS and the GALLBLADDER. | Disorder | Pathology | Digestive System [curated_secondary] | AMW:DIS:060002 |
| Biomass Smoke Exposure Created as a target node for a staged ClinicalGraph edge. Review and enrich this node later if needed. | Risk Factor | Clinical Medicine | Respiratory System [role_derived] | AMW:RISK:115007 |
| Bird Fancier's Lung A form of alveolitis or pneumonitis due to an acquired hypersensitivity to inhaled avian antigens, usually proteins in the dust of bird feathers and … | Immune Disorder | Pathology | Respiratory System [curated_secondary] | AMW:DIS:080048 |
| Birdshot Chorioretinopathy A form of chorioretinitis characterized by multiple small, cream-colored LESIONS, symmetrically scattered mainly around the OPTIC DISK. These lesions… | Immune Disorder | Pathology | Visual System [curated_secondary] | AMW:DIS:110133 |
| Bisphosphonate-Associated Osteonecrosis of the Jaw Necrotic jaws or other maxillofacial skeleton necrosis associated with bisphosphonate use (see BISPHOSPHONATES). Injury, dental procedures, and traum… | Pathologic Condition | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050112 |
| Bladder Exstrophy A birth defect in which the URINARY BLADDER is malformed and exposed, inside out, and protruded through the ABDOMINAL WALL. It is caused by closure d… | Congenital Disorder | Pathology | Renal and Urinary System [curated_secondary] | AMW:DIS:120061 |
| Bland White Garland Syndrome A congenital coronary vessel anomaly in which the left main CORONARY ARTERY originates from the PULMONARY ARTERY instead of from AORTA. The congenita… | Syndrome | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140012 |
| Blepharitis Inflammation of the eyelids. | Inflammatory Disorder | Pathology | Visual System [curated_secondary] | AMW:DIS:110066 |
| Blepharophimosis The abnormal narrowness of the palpebral fissure in the horizontal direction caused by the lateral displacement of the medial canthi of the eyelids. … | Congenital Disorder | Pathology | Visual System [curated_secondary] | AMW:DIS:110029 |
| Blepharoptosis Drooping of the upper lid due to deficient development or paralysis of the levator palpebrae muscle. | Disorder | Pathology | Visual System [curated_secondary] | AMW:DIS:110068 |
| Blepharospasm Excessive winking; tonic or clonic spasm of the orbicularis oculi muscle. | Disorder | Pathology | Visual System [curated_secondary] | AMW:DIS:110069 |
| Blind Loop Syndrome A malabsorption syndrome that is associated with a blind loop in the upper SMALL INTESTINE that is characterized by the lack of peristaltic movement,… | Syndrome | Pathology | Digestive System [curated_secondary] | AMW:DIS:060142 |
| Blindness The inability to see or the loss or absence of perception of visual stimuli. This condition may be the result of EYE DISEASES; OPTIC NERVE DISEASES; … | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100566 |
| Blindness, Cortical Total loss of vision in all or part of the visual field due to bilateral OCCIPITAL LOBE (i.e., VISUAL CORTEX) damage or dysfunction. Anton syndrome i… | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100568 |