| Condition | Indicated | Relationship Strength | Studies | Trials |
|---|
Eye Disorders
[description not available] | 0 | 1.93 | 1 | 0 |
Infection, Toxoplasma gondii
[description not available] | 0 | 1.93 | 1 | 0 |
Ocular Toxoplasmosis
[description not available] | 0 | 1.93 | 1 | 0 |
Eye Diseases
Diseases affecting the eye. | 0 | 1.93 | 1 | 0 |
Toxoplasmosis
The acquired form of infection by Toxoplasma gondii in animals and man. | 0 | 1.93 | 1 | 0 |
Toxoplasmosis, Ocular
Infection caused by the protozoan parasite TOXOPLASMA in which there is extensive connective tissue proliferation, the retina surrounding the lesions remains normal, and the ocular media remain clear. Chorioretinitis may be associated with all forms of toxoplasmosis, but is usually a late sequel of congenital toxoplasmosis. The severe ocular lesions in infants may lead to blindness. | 0 | 1.93 | 1 | 0 |
Libman-Sacks Disease
[description not available] | 0 | 2.66 | 3 | 0 |
Bullous Dermatoses
[description not available] | 0 | 4.14 | 6 | 0 |
Lupus Erythematosus, Systemic
A chronic, relapsing, inflammatory, and often febrile multisystemic disorder of connective tissue, characterized principally by involvement of the skin, joints, kidneys, and serosal membranes. It is of unknown etiology, but is thought to represent a failure of the regulatory mechanisms of the autoimmune system. The disease is marked by a wide range of system dysfunctions, an elevated erythrocyte sedimentation rate, and the formation of LE cells in the blood or bone marrow. | 0 | 2.66 | 3 | 0 |
Hand Dermatosis
[description not available] | 0 | 1.96 | 1 | 0 |
Foot Dermatoses
Skin diseases of the foot, general or unspecified. | 0 | 1.96 | 1 | 0 |
Hand Dermatoses
Skin diseases involving the HANDS. | 0 | 1.96 | 1 | 0 |
Polychondritis, Chronic Atrophic
[description not available] | 0 | 2.37 | 2 | 0 |
Polychondritis, Relapsing
An acquired disease of unknown etiology, chronic course, and tendency to recur. It is characterized by inflammation and degeneration of cartilage and can result in deformities such as floppy ear and saddle nose. Loss of cartilage in the respiratory tract can lead to respiratory obstruction. | 0 | 2.37 | 2 | 0 |
Aortic Arteritis, Giant Cell
[description not available] | 0 | 2.37 | 2 | 0 |
Giant Cell Arteritis
A systemic autoimmune disorder that typically affects medium and large ARTERIES, usually leading to occlusive granulomatous vasculitis with transmural infiltrate containing multinucleated GIANT CELLS. The TEMPORAL ARTERY is commonly involved. This disorder appears primarily in people over the age of 50. Symptoms include FEVER; FATIGUE; HEADACHE; visual impairment; pain in the jaw and tongue; and aggravation of pain by cold temperatures. (From Adams et al., Principles of Neurology, 6th ed) | 0 | 2.37 | 2 | 0 |
Cheilitis Granulomatosa
[description not available] | 0 | 2.9 | 1 | 0 |
Cheilitis
Inflammation of the lips. It is of various etiologies and degrees of pathology. | 0 | 2.9 | 1 | 0 |
Hair Diseases
Diseases affecting the orderly growth and persistence of hair. | 0 | 1.97 | 1 | 0 |
Complications, Pregnancy
[description not available] | 0 | 1.97 | 1 | 0 |
Pregnancy
The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH. | 0 | 2.38 | 2 | 0 |
Carcinoma, Epidermoid
[description not available] | 0 | 2.89 | 1 | 0 |
Cancer of Lung
[description not available] | 0 | 2.89 | 1 | 0 |
Carcinoma, Squamous Cell
A carcinoma derived from stratified SQUAMOUS EPITHELIAL CELLS. It may also occur in sites where glandular or columnar epithelium is normally present. (From Stedman, 25th ed) | 0 | 2.89 | 1 | 0 |
Lung Neoplasms
Tumors or cancer of the LUNG. | 0 | 2.89 | 1 | 0 |
Autoimmune Disease
[description not available] | 0 | 1.97 | 1 | 0 |
Acantholysis Bullosa
[description not available] | 0 | 1.97 | 1 | 0 |
Autoimmune Diseases
Disorders that are characterized by the production of antibodies that react with host tissues or immune effector cells that are autoreactive to endogenous peptides. | 0 | 1.97 | 1 | 0 |
Epidermolysis Bullosa
Group of genetically determined disorders characterized by the blistering of skin and mucosae. There are four major forms: acquired, simple, junctional, and dystrophic. Each of the latter three has several varieties. | 0 | 1.97 | 1 | 0 |
Pemphigus Foliaceus
[description not available] | 0 | 1.97 | 1 | 0 |
Pemphigus
Group of chronic blistering diseases characterized histologically by ACANTHOLYSIS and blister formation within the EPIDERMIS. | 0 | 1.97 | 1 | 0 |
Coxarthrosis
[description not available] | 0 | 1.97 | 1 | 0 |
Osteoarthritis, Hip
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. | 0 | 1.97 | 1 | 0 |
Duhring Disease
[description not available] | 0 | 1.97 | 1 | 0 |
Complications, Infectious Pregnancy
[description not available] | 0 | 1.97 | 1 | 0 |
Dermatitis Herpetiformis
Rare, chronic, papulo-vesicular disease characterized by an intensely pruritic eruption consisting of various combinations of symmetrical, erythematous, papular, vesicular, or bullous lesions. The disease is strongly associated with the presence of HLA-B8 and HLA-DR3 antigens. A variety of different autoantibodies has been detected in small numbers in patients with dermatitis herpetiformis. | 0 | 1.97 | 1 | 0 |