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 |
|---|---|---|---|---|
| Food Intolerance Digestive system disorder where a particular food irritates the digestive tract or cannot be properly digested (i.e., due to a lack of a digestive en… | Pathologic Condition | Pathology | Digestive System [curated_secondary] | AMW:DIS:230304 |
| Foodborne Illness Created as a target node for a staged ClinicalGraph edge. Review and enrich this node later if needed. | Disorder | Pathology | Digestive System [curated_secondary], Respiratory System [role_derived] | AMW:DIS:060238 |
| Foot Deformities Alterations or deviations from normal shape or size which result in a disfigurement of the foot. | Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050147 |
| Foot Deformities, Acquired Distortion or disfigurement of the foot, or a part of the foot, acquired through disease or injury after birth. | Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050148 |
| Foot Deformities, Congenital Alterations or deviations from normal shape or size which result in a disfigurement of the foot occurring at or before birth. | Congenital Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050158 |
| Foot Dermatoses Skin diseases of the foot, general or unspecified. | Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170070 |
| Foot Diseases Anatomical and functional disorders affecting the foot. | Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050164 |
| Foot Ulcer Lesion on the surface of the skin of the foot, usually accompanied by inflammation. The lesion may become infected or necrotic and is frequently asso… | Pathologic Condition | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170071 |
| Foramen Ovale, Patent A condition in which the FORAMEN OVALE in the ATRIAL SEPTUM fails to close shortly after birth. This results in abnormal communications between the t… | Congenital Disorder | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140025 |
| Foveomacular Retinitis A photochemical injury to retina tissues, usually at the RETINAL PIGMENT EPITHELIUM. It is commonly associated with sungazing, eclipse viewing, weldi… | Inflammatory Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100658 |
| Fox-Fordyce Disease Chronic pruritic disease, usually in women, characterized by small follicular papular eruptions in APOCRINE GLANDS areas. It is caused by obstruction… | Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170153 |
| Fracture Dislocation Fracture of a bone near an articulation with concomitant dislocation of that joint. | Traumatic Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050227 |
| Fragile X Syndrome A condition characterized genotypically by mutation of the distal end of the long arm of the X chromosome (at gene loci FRAXA or FRAXE) and phenotypi… | Syndrome | Pathology | Nervous System [curated_secondary] | AMW:DIS:100491 |
| Fraser Syndrome Rare autosomal recessive congenital malformation syndrome characterized by cryptophthalmos, SYNDACTYLY and UROGENITAL ABNORMALITIES. Other anomalies … | Syndrome | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050030 |
| Frasier Syndrome A syndrome characterized by CHRONIC KIDNEY FAILURE and GONADAL DYSGENESIS in phenotypic females with karyotype of 46,XY or female individual with a n… | Syndrome | Pathology | Renal and Urinary System [curated_secondary] | AMW:DIS:120071 |
| Friedreich Ataxia An autosomal recessive disease, usually of childhood onset, characterized pathologically by degeneration of the spinocerebellar tracts, posterior col… | Congenital Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100160 |
| Frontotemporal Dementia The most common clinical form of FRONTOTEMPORAL LOBAR DEGENERATION, this dementia presents with personality and behavioral changes often associated w… | Degenerative Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100232 |
| Frontotemporal Lobar Degeneration The label is process-shaped, but the organ-specific concept may also function as a disorder; manual semantic review is required. | Pathological process | Pathology | Nervous System [curated_secondary] | AMW:PROC:135075 |
| Fuchs' Endothelial Dystrophy Disorder caused by loss of endothelium of the central cornea. It is characterized by hyaline endothelial outgrowths on Descemet's membrane, epithelia… | Congenital Disorder | Pathology | Visual System [curated_secondary] | AMW:DIS:110015 |
| Fucosidosis An autosomal recessive lysosomal storage disease caused by a deficiency of ALPHA-L-FUCOSIDASE activity resulting in an accumulation of fucose contain… | Congenital Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100093 |
| Funnel Chest A developmental anomaly in which the lower sternum is posteriorly dislocated and concavely deformed, resulting in a funnel-shaped thorax. | Congenital Disorder | Pathology | Musculoskeletal System [curated_secondary] | AMW:DIS:050033 |
| Fused Kidney Congenital fusion of two kidneys. | Congenital Disorder | Pathology | Renal and Urinary System [curated_secondary] | AMW:DIS:120083 |
| Gagging Contraction of the muscle of the PHARYNX caused by stimulation of sensory receptors on the SOFT PALATE, by psychic stimuli, or systemically by drugs. | Pathologic Condition | Pathology | Digestive System [curated_secondary] | AMW:DIS:230305 |
| Gait Apraxia Impaired ambulation not attributed to sensory impairment or motor weakness. FRONTAL LOBE disorders; BASAL GANGLIA DISEASES (e.g., PARKINSONIAN DISORD… | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100448 |
| Gait Ataxia Impairment of the ability to coordinate the movements required for normal ambulation (WALKING) which may result from impairments of motor function or… | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100436 |
| Gait Difficulty Created as a target node for a staged ClinicalGraph edge. Review and enrich this node later if needed. | Symptom | Clinical Medicine | Respiratory System [role_derived] | AMW:SYM:185021 |
| Gait Disorders, Neurologic Gait abnormalities that are a manifestation of nervous system dysfunction. These conditions may be caused by a wide variety of disorders which affect… | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100447 |
| Galactorrhea Excessive or inappropriate LACTATION in females or males, and not necessarily related to PREGNANCY. Galactorrhea can occur either unilaterally or bil… | Disorder | Pathology | Reproductive System [curated_secondary] | AMW:DIS:120267 |
| Galactosemias A group of inherited enzyme deficiencies which feature elevations of GALACTOSE in the blood. This condition may be associated with deficiencies of GA… | Congenital Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100079 |
| Gallbladder Diseases Diseases of the GALLBLADDER. They generally involve the impairment of BILE flow, GALLSTONES in the BILIARY TRACT, infections, neoplasms, or other dis… | Disorder | Pathology | Digestive System [curated_secondary] | AMW:DIS:060023 |