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Disease |
Synonyms |
Description |
Articles |
Phenotypes |
endemic goiter
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simple goitre; Iodine-deficiency-related endemic g..
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simple goitre; Iodine-deficiency-related endemic goitre
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A nutritional deficiency disease characterized by .. [+]
A nutritional deficiency disease characterized by noncancerous enlargement of the thyroid gland and has_material_basis_in iodine deficiency.
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Haverhill fever
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Streptobacillosis; Streptobacillary rat-bite fever..
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Streptobacillosis; Streptobacillary rat-bite fever; Streptobacillary fever
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A primary bacterial infectious disease that result.. [+]
A primary bacterial infectious disease that results_in infection, has_material_basis_in Streptobacillus moniliformis, which is transmitted_by contact with urine or secretions from the mouth, eye, or nose of an infected animal or transmitted_by bite of an infected animal, especially rat. The infection has_symptom chills, has_symptom fever, has_symptom rash and has_symptom joint pain.
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chondromalacia patellae
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softening of articular cartilage of patella; Chond..
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softening of articular cartilage of patella; Chondromalacia of patella; Chondromalacia of patella (disorder); Chondromalacia patellae
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n_a
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fibrodysplasia ossificans progressiva
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Stone Man Syndrome; progressive myositis ossifican..
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Stone Man Syndrome; progressive myositis ossificans; myositis ossificans progressiva; progressive ossifying myositis
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A connective tissue disease that is characterized .. [+]
A connective tissue disease that is characterized by progressive ossification of skeletal muscle, fascia, tendons, and ligaments and has_material_basis_in heterozygous mutation in the ACVR1 gene.
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childhood disintegrative disease
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Symbiotic psychosis; Disintegrative psychosis NOS ..
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Symbiotic psychosis; Disintegrative psychosis NOS (disorder); Heller's syndrome; Disintegrative psychosis
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A pervasive developmental disorder that is a rare .. [+]
A pervasive developmental disorder that is a rare condition characterized by late onset (greater than 3 years of age) of developmental delays in language, social function, and motor skills where children who have had previously normal development who then appear to regress.
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purulent labyrinthitis
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Suppurative labyrinthitis (disorder); Suppurative ..
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Suppurative labyrinthitis (disorder); Suppurative labyrinthitis; acute suppurative labyrinthitis; bacterial labyrinthitis
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A labyrinthitis which is a bacterial infectious di.. [+]
A labyrinthitis which is a bacterial infectious disease of the inner ear, often causing deafness and loss of vestibular function. This is caused when bacteria spread to the inner ear during the course of severe acute otitis media, purulent meningitis, or an enlarging cholesteatoma.
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cornea squamous cell carcinoma
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squamous cell carcinoma of cornea (disorder); squa..
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squamous cell carcinoma of cornea (disorder); squamous cell carcinoma of cornea; Corneal Epidermoid carcinoma
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n_a
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acquired tear duct stenosis
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Stenosis of nasolacrimal duct, acquired; acquired ..
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Stenosis of nasolacrimal duct, acquired; acquired nasolacrimal duct stenosis; Tear duct - acquired stenosis; acquired stenosis of nasolacrimal duct
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n_a
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prostate calculus
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Stone of prostate; calculus of prostate; Prostatic..
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Stone of prostate; calculus of prostate; Prostatic stone; Prostatic lithiasis
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n_a
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dermoid cyst of skin
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skin Dermoid; Dermoid cyst of skin (finding); Derm..
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skin Dermoid; Dermoid cyst of skin (finding); Dermoid cyst of skin
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A dermoid cyst that is located_in the skin.
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lymphogranuloma venereum
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Strumous bubo; Durand-Nicolas-Favre disease; Lymph..
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Strumous bubo; Durand-Nicolas-Favre disease; Lymphogranuloma inguinale; Poradenitis inguinale; Climatic or tropical bubo
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A commensal bacterial infectious disease that resu.. [+]
A commensal bacterial infectious disease that results_in infection located_in lymph nodes, has_material_basis_in Chlamydia trachomatis, which is transmitted_by sexual contact, and transmitted_by fomites. The infection has_symptom inguinal lymphadenitis, has_symptom abscesses in the groin area, and has_symptom lymphangitis.
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trochlear nerve disease
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Superior oblique muscle innervation disorder; diso..
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Superior oblique muscle innervation disorder; disorder of trochlear nerve; Trochlear nerve disorder, NOS; Trochlear nerve disorder
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n_a
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nuclear senile cataract
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Senile nuclear cataract; Senile nuclear sclerosis; ..
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Senile nuclear sclerosis; Senile nuclear cataract
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A senile cataract that is characterized by opacifi.. [+]
A senile cataract that is characterized by opacification of the lens nucleus and caused by changes related to aging.
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Tietze's syndrome
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Slipping rib syndrome; Costochondral junction synd..
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Slipping rib syndrome; Costochondral junction syndrome; Costochondritis; Tietze's disease; Costalchondritis; Tietze syndrome
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n_a
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epicondylitis
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shooter's elbow; andrel epicondylitis; archer's el..
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shooter's elbow; andrel epicondylitis; archer's elbow; golfer's elbow; hockey elbow; medial epicondylitis; Lateral epicondylitis; tennis elbow
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A bone inflammation disease that results_in inflam.. [+]
A bone inflammation disease that results_in inflammation located_in epicondyle.
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boutonneuse fever
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South African tick-bite fever; South African tick-..
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South African tick-bite fever; South African tick-bite fever (disorder); african tick typhus; African tick typhus (disorder); Boutonneuse disease; Kenya fever; kenya tick typhus; Mediterranean spotted fever; Mediterranean tick fever; African tick typhus; marseilles fever; Rickettsia conorii spotted fever; Conor and Bruch's disease; Kenyan tick typhus
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A spotted fever that has_material_basis_in Rickett.. [+]
A spotted fever that has_material_basis_in Rickettsia conorii subsp conorii, which is transmitted_by dog tick (Rhipicephalus sanguineus). The infection has_symptom fever, has_symptom eschar (usually single), has_symptom regional adenopathy, has_symptom maculopapular rash on extremities.
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azoospermia
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spermatogenic failure
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A male infertility disease characterized by the ab.. [+]
A male infertility disease characterized by the absence of any measurable level of sperm in semen.
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46,XY sex reversal
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Swyer syndrome; 46,XY SEX REVERSAL; Pure gonadal d..
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Swyer syndrome; 46,XY SEX REVERSAL; Pure gonadal dysgenesis 46,XY; 46 XY gonadal dysgenesis
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A gonadal dysgenesis that is characterized by a no.. [+]
A gonadal dysgenesis that is characterized by a normal 46,XY karyotype along with a progressive loss of germ cells on the developing gonads of an embryo.
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Niemann-Pick disease
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Sphingomyelinase Deficiency Disease; sphingomyelin..
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Sphingomyelinase Deficiency Disease; sphingomyelin lipidosis; lipoid histiocytosis (classical phosphatide); Niemann-Pick disease type A; Niemann-Pick disease type B; Niemann-Pick disease type C; Niemann-Pick disease with cholesterol esterification block; Niemann-Pick disease, subacute juvenile form; Type A Niemann-Pick Disease; lipoid histiocytosis
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A sphingoliidosis characterized by the accumulatio.. [+]
A sphingoliidosis characterized by the accumulation of the lipid sphingomyelin in lysosomes in cells.
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trichorhinophalangeal syndrome type I
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Sugio-Kajii syndrome; type I trichorhinophalangeal..
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Sugio-Kajii syndrome; type I trichorhinophalangeal syndrome; type III trichorhinophalangeal syndrome; Trichorhinophalangeal dysplasia type I; trichorhinophalangeal syndrome type 1
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A syndrome that is characterized by short stature,.. [+]
A syndrome that is characterized by short stature, sparse hair, a bulbous nasal tip and cone-shaped epiphyses (the growing ends of bones), as well as severe generalized shortening of all finger and toe bones (brachydactyly).
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calcaneonavicular coalition
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SYNOSTOSES, TARSAL, CARPAL AND DIGITAL; Multiple s..
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SYNOSTOSES, TARSAL, CARPAL AND DIGITAL; Multiple synostosis syndrome (disorder); Multiple synostosis syndrome
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A synostosis characterized by the fusion of carpal.. [+]
A synostosis characterized by the fusion of carpal and tarsal bones, which causes stiffness and immobility of the hands and the feet.
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African tick-bite fever
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south african tick-bite fever; Rickettsia africae ..
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south african tick-bite fever; Rickettsia africae spotted fever
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A spotted fever that has_material_basis_in Rickett.. [+]
A spotted fever that has_material_basis_in Rickettsia africae, which is transmitted_by ticks (Amblyomma hebraeum and Amblyomma variegatum). The infection has_symptom fever, has_symptom eschar and has_symptom maculopapular rash.
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Rocky Mountain spotted fever
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Sao Paulo typhus; So Paulo fever; Brazillian spott..
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So Paulo fever; Sao Paulo typhus; Brazillian spotted; Choix; Exanthematic typhus of Sao Paulo; Fiebre maculosa; Fiebre manchada; Tick typhus; Tobia fever; Brazilian spotted
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A spotted fever that has_material_basis_in Rickett.. [+]
A spotted fever that has_material_basis_in Rickettsia rickettsii, which is transmitted_by ticks (Dermacentor variabilis and Dermacentor andersoni). The infection has_symptom fever, has_symptom headache, has_symptom abdominal pain, and has_symptom maculopapular rash progressing into papular or petechial rash.
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otomycosis
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Singapore ear
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An otitis externa which is a disease of the ear pr.. [+]
An otitis externa which is a disease of the ear produced by the growth of fungi in the external auditory canal. It is characterized by inflammation, pruritus, scaling and severe discomfort. The most common fungi are Aspergillus niger and Candida albicans.
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autoimmune polyendocrine syndrome type 2
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Schmidt syndrome
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An autoimmune polyendocrine syndrome that is chara.. [+]
An autoimmune polyendocrine syndrome that is characterized by abnormal functioning of the immune system that causes auto-reactivity against endocrine organs. It is more heterogeneous and has not been linked to one gene.
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tick-borne encephalitis
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Siberian tick-borne encephalitis; Russian spring-s..
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Siberian tick-borne encephalitis; Russian spring-summer encephalitis; west-Siberian encephalitis; Western European tick-borne encephalitis; Central European encephalitis; Taiga encephalitis; Far Eastern TBE
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A viral infectious disease that results_in inflamm.. [+]
A viral infectious disease that results_in inflammation located_in brain, has_material_basis_in Tick-borne encephalitis virus, which is transmitted_by Ixodes ticks. The infection has_symptom drowsiness, has_symptom confusion, has_symptom sensory disturbances, and has_symptom paralysis.
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multiple endocrine neoplasia type 2A
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Sipple syndrome; multiple endocrine neoplasia II; ..
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Sipple syndrome; multiple endocrine neoplasia II; MEN2A
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A multiple endocrine neoplasia characterized by me.. [+]
A multiple endocrine neoplasia characterized by medullary carcinoma of the thyroid, pheochromocytoma, hyperparathyroidism, and occasionally cutaneous lichen amyloidosis.
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mucosulfatidosis
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Sulfatidosis, Juvenile, Austin Type; multiple sulf..
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Sulfatidosis, Juvenile, Austin Type; multiple sulfatase deficiency disease
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A sphingolipidosis that is characterized by leukod.. [+]
A sphingolipidosis that is characterized by leukodystrophy, ichthyosis, skeletal abnormalities and shortened life expectancy and has_material_basis_in mutation in the SUMF1 gene that results in deficiency in multiple sulfatase enzymes.
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Brugada syndrome
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SUNDS; sudden unexplained nocturnal death syndrome..
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SUNDS; sudden unexplained nocturnal death syndrome; Brugada type idiopathic ventricular fibrillation; Pokkuri death syndrome; Dream disease; Bangungut
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A heart conduction disease that is characterized b.. [+]
A heart conduction disease that is characterized by abnormal electrocardiogram (ECG) findings and an increased risk of sudden cardiac death.
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4 articles
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Buruli ulcer disease
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Searle's ulcer; Searl ulcer; Bairnsdale ulcer; Dai..
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Searl ulcer; Searle's ulcer; Bairnsdale ulcer; Daintree ulcer; Mossman ulcer
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A primary bacterial infectious disease that result.. [+]
A primary bacterial infectious disease that results_in infection located_in skin or located_in subcutaneous tissue, has_material_basis_in Mycobacterium ulcerans, which could be transmitted_by insects. The bacterium produces a toxin, named mycolactone, which causes subcutaneous fat necrosis and inhibits an immune response. The infection has_symptom nodule, which is a painless, mobile swelling in the skin.
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Weill-Marchesani syndrome
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Spherophakia Brachymorphia Syndrome; congenital me..
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Spherophakia Brachymorphia Syndrome; congenital mesodermal dystrophy; Mesodermal Dysmorphodystrophy, Congenital; GEMSS syndrome; Marchesani-Weill Syndrome
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A syndrome characterized by short stature, brachyc.. [+]
A syndrome characterized by short stature, brachycephaly and other facial abnormalities, brachydactyly, joint stiffness and distinctive ocular abnormalities.
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epidemic typhus
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sylvatic typhus
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A typhus that has_material_basis_in Rickettsia pro.. [+]
A typhus that has_material_basis_in Rickettsia prowazekii, which is transmitted by human body louse (Pediculus humanus corporis). The infection has_symptom high fever, has_symptom cough, has_symptom rash, has_symptom severe muscle pain, has_symptom chills, has_symptom falling blood pressure, has_symptom stupor, has_symptom sensitivity to light, and has_symptom delirium.
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endemic typhus
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Shop typhus; cat flea rickettsiosis; fleaborne typ..
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Shop typhus; cat flea rickettsiosis; fleaborne typhus; murine typhus; Rat-Flea Typhus; Rickettsia felis spotted fever; toulon typhus; urban typhus; Urban Typhus of Malaya
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A typhus that has_material_basis_in Rickettsia typ.. [+]
A typhus that has_material_basis_in Rickettsia typhi or has_material_basis_in Rickettsia felis, which are transmitted by fleas (Xenopsylla cheopis). The infection has symptom headache, has symptom fever, has symptom chills, has symptom myalgia, has symptom nausea, has symptom vomiting, has symptom cough and has symptom rash.
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exanthema subitum
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Sixth Disease; Roseola Infantum
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A viral infectious disease that results_in infecti.. [+]
A viral infectious disease that results_in infection in infants and children, located_in skin, has_material_basis_in Human herpesvirus 6 or has_material_basis_in Human herpesvirus 7 and has_symptom sudden high fever, and has_symptom red rash that occurs first on the trunk then spreading to legs and neck.
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adult spinal muscular atrophy
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SPINAL MUSCULAR ATROPHY, ADULT FORM; spinal muscul..
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SPINAL MUSCULAR ATROPHY, ADULT FORM; spinal muscular atrophy 4; SMA4; SPINAL MUSCULAR ATROPHY, TYPE IV
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A spinal muscular atrophy that is characterized by.. [+]
A spinal muscular atrophy that is characterized by progressive muscular weakness and motor disability that typically presents in the third decade of life and has_material_basis_in mutations in the SMN1 or SMN2 genes that are required for the survival of motor neurons.
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1 articles
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intermediate spinal muscular atrophy
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spinal muscular atrophy type II; SMA2; spinal musc..
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SMA2; spinal muscular atrophy type II; spinal muscular atrophy 2; SMA II; MUSCULAR ATROPHY, SPINAL, INFANTILE CHRONIC FORM; MUSCULAR ATROPHY, SPINAL, INTERMEDIATE TYPE
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A childhood spinal muscular atrophy that is charac.. [+]
A childhood spinal muscular atrophy that is characterized by progressive muscular weakness and respiratory failure, develops in children between the ages of 6 and 12 months and drastically reduces length of life, and has_material_basis_in mutations in the SMN1 or SMN2 genes that are required for the survival of motor neurons.
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visceral heterotaxy
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situs ambiguus; heterotaxia
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A physical disorder characterized by the abnormal .. [+]
A physical disorder characterized by the abnormal distribution of the major visceral organs within the chest and abdomen.
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34 articles
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121 matches
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congenital disorder of glycosylation type I
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SRD5A3-CDG (CDG-1q); ALG1-CDG (CDG-1k); ALG11-CDG ..
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SRD5A3-CDG (CDG-1q); ALG1-CDG (CDG-1k); ALG11-CDG (CDG-1p); ALG2-CDG (CDG-1i); ALG3-CDG (CDG-1d); ALG6-CDG (CDG-1c); ALG8-CDG (CDG-1h); ALG9-CDG (CDG-1l); DPAGT1-CDG (CDG-1j); DPM1-CDG (CDG-1e); DPM2-CDG (CDG-1u); DPM3-CDG (CDG-1o); MPDU1-CDG (CDG-1f); PMM2-CDG (CDG-1a); RFT1-CDG (CDG-1n); ALG12-CDG (CDG-1g); DOLK-CDG (CDG-1m); MPI-CDG (CDG-1b)
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A congenital disorder of glycosylation characteriz.. [+]
A congenital disorder of glycosylation characterized by under-glycosylated serum glycoproteins.
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cranioectodermal dysplasia
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Sensenbrenner syndrome; Levin syndrome; cranioecto..
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Sensenbrenner syndrome; Levin syndrome; cranioectodermal dysplasia
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A syndrome that is characterized by characterized .. [+]
A syndrome that is characterized by characterized by sagittal craniosynostosis and facial, ectodermal, and skeletal anomalies.
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1 articles
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tooth agenesis
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selective tooth agenesis; hypodontia; oligodontia; ..
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selective tooth agenesis; hypodontia; oligodontia; familial tooth agenesis
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A tooth disease characterized by failure to develo.. [+]
A tooth disease characterized by failure to develop one or more missing teeth.
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1 articles
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asphyxiating thoracic dystrophy
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short-rib thoracic dysplasia with or without polyd..
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short-rib thoracic dysplasia with or without polydactyly; Jeune syndrome; thoracic pelvic phalangeal dystrophy
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A bone development disease characterized by skelet.. [+]
A bone development disease characterized by skeletal abnormalities and resulting in difficulty in breathing caused by mutations that result in ciliopathy.
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1 articles
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intestinal schistosomiasis
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Schistosoma mansoni infectious disease; schistosom..
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Schistosoma mansoni infectious disease; schistosomiasis japonica; Schistosoma japonicum infection; Katayama fever
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A schistosomiasis that involves parasitic infectio.. [+]
A schistosomiasis that involves parasitic infection of the intestine caused by Schistosoma mansoni, Schistosoma intercalatum or Schistosomiasis japonicum. The symptoms include fever, cough, abdominal pain, diarrhea, hepatosplenomegaly, colonic polyposis with bloody diarrhea and eosinophilia.
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paranasal sinus cancer
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squamous cell carcinoma of paranasal sinus; adenoi..
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squamous cell carcinoma of paranasal sinus; adenoid cystic carcinoma of Accessory sinus; Epidermoid carcinoma of the paranasal sinus; Mucoepidermoid carcinoma of Accessory sinus; paranasal sinus adenocarcinoma; paranasal sinus squamous cell carcinoma; paranasal sinus mucoepidermoid carcinoma; adenoid cystic carcinoma of paranasal sinus; paranasal sinus adenoid cystic carcinoma
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A respiratory system cancer that is located_in the.. [+]
A respiratory system cancer that is located_in the paranasal sinuses.
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familial visceral amyloidosis
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systemic nonneuropathic amyloidosis; AMYLOIDOSIS, ..
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systemic nonneuropathic amyloidosis; AMYLOIDOSIS, FAMILIAL RENAL; German type amyloidosis; OSTERTAG TYPE AMYLOIDOSIS
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An amyloidosis that is characterized by the abnorm.. [+]
An amyloidosis that is characterized by the abnormal deposition of amyloid proteins that is located_in the visceral organs, primarily the kidneys.
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anauxetic dysplasia 1
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spondylometaepiphyseal dysplasia, Menger type
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An anauxetic dysplasia that has_material_basis_in .. [+]
An anauxetic dysplasia that has_material_basis_in homozygous or compound heterozygous mutation in the RMRP gene on chromosome 9p13.
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distal arthrogryposis
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Sheldon-Hall syndrome; Arthrogryposis Multiplex Co..
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Sheldon-Hall syndrome; Arthrogryposis Multiplex Congenita; Freeman-Sheldon syndrome; Freeman-Sheldon syndrome variant
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A muscle tissue disease characterized by congenita.. [+]
A muscle tissue disease characterized by congenital joint contractures of hand and feet.
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3 articles
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Arts syndrome
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syndromic X-linked mental retardation Arts type; s..
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syndromic X-linked mental retardation Arts type; syndromic X-linked mental retardation 18; ARTS; fatal X-linked ataxia with deafness and loss of vision; MRXSARTS; Lethal ataxia with deafness and optic atrophy; MRXS18
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An X-linked disease that is characterized by profo.. [+]
An X-linked disease that is characterized by profound congenital sensorineural hearing impairment, early-onset hypotonia, delayed motor development, mild to moderate intellectual disability, ataxia, and increased risk of infection and has_material_basis_in mutations of the PRPS1 gene.
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alcohol-related neurodevelopmental disorder
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static encephalopathy; ARND
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A fetal alcohol spectrum disorder that results in .. [+]
A fetal alcohol spectrum disorder that results in central nervous system dysfunction and behavioral and/or cognitive deficits due to prenatal alcohol exposure.
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Borjeson-Forssman-Lehmann syndrome
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syndromic X-linked mental retardation Borjeson-For..
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syndromic X-linked mental retardation Borjeson-Forssman-Lehmann type; BORJ; Borjeson syndrome; mental retardation, epilepsy, and endocrine disorder; MRXSBFL; BFLS; intellectual deficiency-epilepsy-endocrine disorders syndrome
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An X-linked disease that is characterized by intel.. [+]
An X-linked disease that is characterized by intellectual disability, truncal obesity, seizures, hypogonadism, developmental delay, distinctive facial features, tapered fingers and short toes and has_material_basis_in X-linked recessive inheritance of mutations in the PHF6 gene.
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Brooke-Spiegler syndrome
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Spiegler-Brooke Syndrome; SBS; BRSS; BSS; CYLD cut..
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SBS; Spiegler-Brooke Syndrome; BRSS; BSS; CYLD cutaneous syndrome
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A skin disease that is characterized by the develo.. [+]
A skin disease that is characterized by the development of several types of tumors from the skin, has_material_basis_in heterozygous mutation in the CYLD gene on chromosome 16q12.
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