Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
viral exanthem	EFO_1000776	[a virus-induced exanthem, A virus-induced exanthem]
toxicodendron dermatitis	EFO_1000773	[An allergic contact dermatitis caused by exposure to plants of the genus Toxicodendron (formerly Rhus). These include poison ivy, poison oak, and poison sumac, all plants that contain the substance urushiol, a potent skin sensitizing agent. (From Dorland, 27th ed), an allergic contact dermatitis (allergic phytodermatitis) that occurs from exposure to members of the plant genus Toxicodendron.]
vesiculobullous skin disease	EFO_1000774	[Skin diseases characterized by local or general distributions of blisters. They are classified according to the site and mode of blister formation. Lesions can appear spontaneously or be precipitated by infection, trauma, or sunlight. Etiologies include immunologic and genetic factors. (From Scientific American Medicine, 1990), Skin diseases characterized by local or general distributions of vesicles and bullae (i.e. blisters). Both vesicles and bullae are fluid-filled lesions, distinguished by size (vesicles being less than 5–10 mm and bullae being larger than 5–10 mm). Vesiculobullous diseases are classified according to the site and mode of blister formation. Lesions can appear spontaneously or be precipitated by infection, trauma, or sunlight. Etiologies include immunologic and genetic factors. In the case of vesiculobullous diseases which are also immune disorders, the term immunobullous is sometimes used. (From Scientific American Medicine, 1990, and Wikipedia)]
subcorneal pustular dermatosis	EFO_1000771	[a rare, benign, chronic relapsing sterile pustular eruption typically involving the flexural sites of the trunk and proximal extremities. It most commonly affects woman aged 40 years or older., A rare, benign, chronic disease characterized by sterile pustular eruption, typically involving the flexural sites of the trunk and proximal extremities.]
stromal corneal pigmentation	EFO_1000770	[stromal pigmentation such as that in ochronosis results from chronic irritation. The melanin is in the superficial stroma and the basal layer of the corneal epithelium., Stromal pigmentation such as that in ochronosis results from chronic irritation. The melanin is in the superficial stroma and the basal layer of the corneal epithelium.]
corneal deposit	MONDO_0001308
vulvar seborrheic keratosis	EFO_1000779	[pigmented vulvar lesions categorized with seborrheic keratosis, A benign squamous neoplasm that arises from the vulva. It is characterized by the proliferation of the basal cells in the squamous epithelium, acanthosis, hyperkeratosis, and cysts formation.]
vulva fibroepithelial polyp	EFO_1000777	[Polyp composed of a central core of fibrous tissue containing irregular shaped thin walled vessels and stellate cells. The overlying squamous epithelium may display reactive changes, but without papillomatous architecture or koilocytosis, A polypoid lesion that arises from the vulva and is characterized by the presence of fibrovascular stroma lined by squamous epithelium. There is no evidence of epithelial atypia.]
polyp of vulva	MONDO_0021396	[A polyp that involves the mammalian vulva.]
female genital tract polyp	EFO_0008622	[A soft and painless polypoid mass that arises from the female genital tract.]
fibroepithelial polyp	MONDO_0060765	[A polypoid lesion composed of fibrous tissue and epithelium. Representative examples include skin tag, anal fibroepithelial polyp, and gingival fibroepithelial polyp.]
vulvar inverted follicular keratosis	EFO_1000778	[Inverted follicular keratosis of the vulvar skin, Seborrheic keratosis that arises from follicular structures in the vulva. It is characterized by the presence of prominent squamous eddies.]
osteoarthritis, hip	EFO_1000786	[Noninflammatory degenerative disease of the hip joint which usually appears in late middle or old age. It is characterized by growth or maturational disturbances in the femoral neck and head, as well as acetabular dysplasia. A dominant symptom is pain on weight-bearing or motion., Osteoarthritis of the hip is also very common and can affect either one or both hips. You’re most likely to feel pain deep at the front of your groin, but also at the side and front of your thigh, in your buttock or down to your knee (this is called radiated pain). If you have severe hip osteoarthritis, you may find your affected leg seems a little shorter than the other because of the bone on either side of your joint being crunched up. ]
osteoarthritis	MONDO_0005178	[A noninflammatory degenerative joint disease occurring chiefly in older persons, characterised by degeneration of the articular cartilage, hypertrophy of bone at the margins and changes in the synovial membrane. It is accompanied by pain and stiffness, particularly after prolonged activity.]
osteoarthritis, spine	EFO_1000787	[A degenerative joint disease involving the spine. It is characterized by progressive deterioration of the spinal articular cartilage (cartilage, articular), usually with hardening of the subchondral bone and outgrowth of bone spurs (osteophyte)., Changes that affect the bones of your spine and the discs between the bones are often called spondylosis, but they’re very similar to the changes caused by osteoarthritis in other joints. X-rays show that spondylosis is extremely common, but it’s not the most common cause of back pain or neck pain and often doesn’t cause any problems at all.]
microscopic polyangiitis	EFO_1000784	[A primary systemic vasculitis of small- and some medium-sized vessels. It is characterized by a tropism for kidneys and lungs, positive association with anti-neutrophil cytoplasmic antibodies (ANCA), and a paucity of immunoglobulin deposits in vessel walls., Microscopic polyangiitis (MPA) is an inflammatory, necrotizing, systemic vasculitis that affects predominantly small vessels (i.e. small arteries, arterioles, capillaries, venules) in multiple organs.]
secondary glomerular disease	MONDO_0019724	[Secondary glomerular diseases are conditions with glomerular pathology in which an underlying cause can be established.]
Anti-neutrophil cytoplasmic antibody-associated vasculitis	MONDO_0015492	[Group of systemic vasculitis with a strong association with anca. The disorders are characterized by necrotizing inflammation of small and medium size vessels, with little or no immune-complex deposits in vessel walls.]
Arteritis	EFO_0009011	[An inflammatory process affecting an artery., An inflammatory process affecting an artery. [ NCI ]]
Sezary's disease	EFO_1000785	[Sezary syndrome (SS) is an aggressive form of cutaneous T-cell lymphoma characterized by a triad of erythroderma, lymphadenopathy and circulating atypical lymphocytes (Sezary cells).]