| Condition | Indicated | Relationship Strength | Studies | Trials |
|---|
Autosomal Dominant Cerebellar Ataxia, Type II
[description not available] | 0 | 2.41 | 1 | 0 |
Spinocerebellar Ataxias
A group of predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43) | 0 | 2.41 | 1 | 0 |
Collodion Baby Syndrome
[description not available] | 0 | 2.25 | 1 | 0 |
Dermatitis Exfoliativa
[description not available] | 0 | 4.4 | 7 | 0 |
Genetic Skin Diseases
[description not available] | 0 | 2.25 | 1 | 0 |
Hand Dermatosis
[description not available] | 0 | 3.5 | 2 | 0 |
Foot Dermatoses
Skin diseases of the foot, general or unspecified. | 0 | 3.5 | 2 | 0 |
Dermatitis, Exfoliative
The widespread involvement of the skin by a scaly, erythematous dermatitis occurring either as a secondary or reactive process to an underlying cutaneous disorder (e.g., atopic dermatitis, psoriasis, etc.), or as a primary or idiopathic disease. It is often associated with the loss of hair and nails, hyperkeratosis of the palms and soles, and pruritus. (From Dorland, 27th ed) | 0 | 4.4 | 7 | 0 |
Hand Dermatoses
Skin diseases involving the HANDS. | 0 | 3.5 | 2 | 0 |
Ichthyosis, Lamellar
A chronic, congenital ichthyosis inherited as an autosomal recessive trait. Infants are usually born encased in a collodion membrane which sheds within a few weeks. Scaling is generalized and marked with grayish-brown quadrilateral scales, adherent at their centers and free at the edges. In some cases, scales are so thick that they resemble armored plate. | 0 | 2.25 | 1 | 0 |
Dermatoses
[description not available] | 0 | 5.41 | 13 | 0 |
Skin Diseases
Diseases involving the DERMIS or EPIDERMIS. | 0 | 5.41 | 13 | 0 |
Dementia Praecox
[description not available] | 0 | 2.55 | 2 | 0 |
Schizophrenia
A severe emotional disorder of psychotic depth characteristically marked by a retreat from reality with delusion formation, HALLUCINATIONS, emotional disharmony, and regressive behavior. | 0 | 2.55 | 2 | 0 |
Celiac Sprue
[description not available] | 0 | 3.09 | 1 | 0 |
Disease Models, Animal
Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases. | 0 | 3.09 | 1 | 0 |
Duhring Disease
[description not available] | 0 | 3.09 | 1 | 0 |
Celiac Disease
A malabsorption syndrome that is precipitated by the ingestion of foods containing GLUTEN, such as wheat, rye, and barley. It is characterized by INFLAMMATION of the SMALL INTESTINE, loss of MICROVILLI structure, failed INTESTINAL ABSORPTION, and MALNUTRITION. | 0 | 3.09 | 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 | 3.09 | 1 | 0 |
Acantholysis Bullosa
[description not available] | 0 | 2.5 | 2 | 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 | 2.5 | 2 | 0 |
Incontinentia Pigmenti Achromians
[description not available] | 0 | 4.25 | 6 | 0 |
EBS-DM
[description not available] | 0 | 2.1 | 1 | 0 |
Epidermolysis Bullosa Simplex
A form of epidermolysis bullosa characterized by serous bullae that heal without scarring. Mutations in the genes that encode KERATIN-5 and KERATIN-14 have been associated with several subtypes of epidermolysis bullosa simplex. | 0 | 2.1 | 1 | 0 |
Hyperidrosis
[description not available] | 0 | 2.1 | 1 | 0 |
Hyperhidrosis
Excessive sweating. In the localized type, the most frequent sites are the palms, soles, axillae, inguinal folds, and the perineal area. Its chief cause is thought to be emotional. Generalized hyperhidrosis may be induced by a hot, humid environment, by fever, or by vigorous exercise. | 0 | 2.1 | 1 | 0 |
Congenital Limb Deformities
[description not available] | 0 | 3.03 | 1 | 0 |
Anodontia
Congenital absence of the teeth; it may involve all (total anodontia) or only some of the teeth (partial anodontia, hypodontia), and both the deciduous and the permanent dentition, or only teeth of the permanent dentition. (Dorland, 27th ed) | 0 | 3.03 | 1 | 0 |
Nail Abnormalities
[description not available] | 0 | 3.03 | 1 | 0 |
Anhidrotic Ectodermal Dysplasia
[description not available] | 0 | 3.03 | 1 | 0 |
Lacrimal Duct Obstruction
Interference with the secretion of tears by the lacrimal glands. Obstruction of the LACRIMAL SAC or NASOLACRIMAL DUCT causing acute or chronic inflammation of the lacrimal sac (DACRYOCYSTITIS). It is caused also in infants by failure of the nasolacrimal duct to open into the inferior meatus and occurs about the third week of life. In adults occlusion may occur spontaneously or after injury or nasal disease. (Newell, Ophthalmology: Principles and Concepts, 7th ed, p250) | 0 | 3.03 | 1 | 0 |
Genetic Predisposition
[description not available] | 0 | 2.77 | 3 | 0 |
Psychoses
[description not available] | 0 | 2.13 | 1 | 0 |
Psychotic Disorders
Disorders in which there is a loss of ego boundaries or a gross impairment in reality testing with delusions or prominent hallucinations. (From DSM-IV, 1994) | 0 | 2.13 | 1 | 0 |
Symptom Cluster
[description not available] | 0 | 4.06 | 5 | 0 |
Syndrome
A characteristic symptom complex. | 0 | 4.06 | 5 | 0 |
Bleb
[description not available] | 0 | 2.05 | 1 | 0 |
Erythema
Redness of the skin produced by congestion of the capillaries. This condition may result from a variety of disease processes. | 0 | 2.05 | 1 | 0 |
Skin Aging
The process of aging due to changes in the structure and elasticity of the skin over time. It may be a part of physiological aging or it may be due to the effects of ultraviolet radiation, usually through exposure to sunlight. | 0 | 2.05 | 1 | 0 |
Xeroderma
[description not available] | 0 | 2.97 | 1 | 0 |
Ichthyosis
Any of several generalized skin disorders characterized by dryness, roughness, and scaliness, due to hypertrophy of the stratum corneum epidermis. Most are genetic, but some are acquired, developing in association with other systemic disease or genetic syndrome. | 0 | 2.97 | 1 | 0 |
Hypoproteinemia
A condition in which total serum protein level is below the normal range. Hypoproteinemia can be caused by protein malabsorption in the gastrointestinal tract, EDEMA, or PROTEINURIA. | 0 | 2.05 | 1 | 0 |
Bullous Congenital Ichthyosiform Erythroderma
[description not available] | 0 | 2.43 | 2 | 0 |
Bullous Dermatoses
[description not available] | 0 | 2.07 | 1 | 0 |
Eczema, Atopic
[description not available] | 0 | 2.07 | 1 | 0 |
Dermatitis, Atopic
A chronic inflammatory genetically determined disease of the skin marked by increased ability to form reagin (IgE), with increased susceptibility to allergic rhinitis and asthma, and hereditary disposition to a lowered threshold for pruritus. It is manifested by lichenification, excoriation, and crusting, mainly on the flexural surfaces of the elbow and knee. In infants it is known as infantile eczema. | 0 | 2.07 | 1 | 0 |
Palmoplantaris Pustulosis
[description not available] | 0 | 2.01 | 1 | 0 |
Ichthyosis Simplex
[description not available] | 0 | 2.01 | 1 | 0 |
Psoriasis
A common genetically determined, chronic, inflammatory skin disease characterized by rounded erythematous, dry, scaling patches. The lesions have a predilection for nails, scalp, genitalia, extensor surfaces, and the lumbosacral region. Accelerated epidermopoiesis is considered to be the fundamental pathologic feature in psoriasis. | 0 | 2.01 | 1 | 0 |