Search Diseases
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Disease | Synonyms | Description | Articles | Phenotypes |
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carbapenem allergy |
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A drug allergy that has_allergic_trigger carbapene..[+]
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co-trimoxazole allergy |
cotrimoxazol allergy; Bactrim allergy; TMP/SMX all..
[+]
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A drug allergy that has_allergic_trigger co-trimox..[+]
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Chlamydia pneumonia |
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A bacterial pneumonia has_material_basis_in Chlamy..[+]
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chikungunya |
Chikungunya fever
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A viral infectious disease that results_in infecti..[+]
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cutaneous mycosis |
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A fungal infectious disease that results_in infect..[+]
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cryptogenic organizing pneumonia |
An idiopathic interstitial pneumonia characterized..[+]
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cutaneous lupus erythematosus |
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A lupus erythematosus that causes skin lesions on ..[+]
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Chapare hemorrhagic fever |
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A viral infectious disease that is a hemorrhagic f..[+]
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coenurosis |
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A parasitic helminthiasis infectious disease that ..[+]
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conidiobolomycosis |
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An subcutaneous mycosis that is a chronic inflamma..[+]
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congenital hypothyroidism |
cretinism
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A hypothyroidism that is present at birth.
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1 articles | 3 matches |
commensal bacterial infectious disease |
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A bacterial infectious disease that results_in inf..[+]
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1 articles | |
Carrion's disease |
Carrion disease; Oroya fever
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A bartonellosis that results_in infection located_..[+]
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complement factor I deficiency |
A complement deficiency that is characterized by r..[+]
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campomelic dysplasia |
Acampomelic Campomelic Dysplasia
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An osteochondrodysplasia that has_material_basis_i..[+]
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3 articles | |
Costello syndrome |
Faciocutaneoskeletal Syndrome; FCS SYNDROME
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A RASopathy characterized by craniofacial dysmorph..[+]
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1 articles | |
Carney complex |
A syndrome characterized by myxomas, spotty pigmen..[+]
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congenital stationary night blindness |
congenital essential nyctalopia
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A hereditary night blindness that is characterized..[+]
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Charcot-Marie-Tooth disease type 1 |
hereditary motor and sensory neuropathy type 1
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A Charcot-Marie-Tooth disease characterized by dem..[+]
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1 articles | |
Charcot-Marie-Tooth disease type 2 |
hereditary motor and sensory neuropathy Guadalajar..
[+]
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A Charcot-Marie-Tooth disease characterized by abn..[+]
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1 articles | |
Charcot-Marie-Tooth disease type 3 |
DEJERINE-SOTTAS SYNDROME; DEJERINE-SOTTAS NEUROPAT..
[+]
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A Charcot-Marie-Tooth disease that is characterize..[+]
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Charcot-Marie-Tooth disease type 4 |
hereditary motor and sensory neuropathy
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A Charcot-Marie-Tooth disease characterized by dem..[+]
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Charcot-Marie-Tooth disease type X |
COWCK; Cowchock syndrome
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A Charcot-Marie-Tooth disease that has_material_ba..[+]
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1 articles | |
Charcot-Marie-Tooth disease intermediate type |
Charcot-Marie-Tooth disease dominant intermediate; ..
[+]
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A Charcot-Marie-Tooth disease characterized by mot..[+]
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congenital adrenal insufficiency |
ADRENAL INSUFFICIENCY, CONGENITAL, WITH 46,XY SEX ..
[+]
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An adrenal gland disease that is characterized by ..[+]
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congenital muscular dystrophy |
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A muscular dystrophy that is characterized by dimi..[+]
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1 articles | |
congenital disorder of glycosylation type I |
ALG1-CDG (CDG-1k); ALG11-CDG (CDG-1p); ALG2-CDG (C..
[+]
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A congenital disorder of glycosylation characteriz..[+]
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congenital disorder of glycosylation type II |
B4GALT1-CDG (CDG-2d); MOGS-CDG (CDG-2b); MGAT2-CDG..
[+]
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A congenital disorder of glycosylation that involv..[+]
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cone-rod dystrophy |
cone-rod retinal dystrophy
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A retinal degeneration that characterized by progr..[+]
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1 articles | |
cranioectodermal dysplasia |
cranioectodermal dysplasia; Levin syndrome; Sensen..
[+]
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A syndrome that is characterized by characterized ..[+]
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1 articles | |
congenital generalized lipodystrophy |
Beradinelli-Seip syndrome
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A lipodystrophy that is characterized by extreme s..[+]
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congenital bile acid synthesis defect |
cholestasis with delta(4)-3-oxosteroid-5-beta-redu..
[+]
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A steroid inherited metabolic disorder characteriz..[+]
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cell type cancer |
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A cancer that is classified by the type of cell fr..[+]
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31 articles | 30 matches |
chorioamnionitis |
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A placenta disease that is an inflammation of the ..[+]
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cardiomyopathy |
Cardiomyopathies
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A heart disease and a myopathy that is characteriz..[+]
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45 articles | |
childhood electroclinical syndrome |
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An electroclinical syndrome with onset in childhoo..[+]
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5 articles | |
COX deficiency, infantile mitochondrial myopathy |
cardioencephalomyopathy, fatal infantile, due to c..
[+]
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A cytochrome-c oxidase deficiency disease characte..[+]
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cerebral folate receptor alpha deficiency |
Neurodegeneration due to cerebral folate transport..
[+]
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A vitamin metabolic disorder that has_material_bas..[+]
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Chanarin-Dorfman syndrome |
Chanarin-Dorfman syndrome; neutral lipid storage d..
[+]
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A lipid storage disease that is characterized by a..[+]
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coenzyme Q10 deficiency disease |
COENZYME Q10 DEFICIENCY, PRIMARY
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A mitochondrial metabolism disease that is charact..[+]
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congenital intrinsic factor deficiency |
hereditary intrinsic factor deficiency
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A vitamin B12 deficiency that is characterized by ..[+]
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cerebellar ataxia |
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A cerebellar disease characterized by ataxia origi..[+]
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5 articles | |
choreaacanthocytosis |
A neuroacanthocytosis characterized by progressive..[+]
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cone dystrophy |
retinal cone dystrophy
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A retinal disease that is characterized by the los..[+]
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1 articles | |
cerebral creatine deficiency syndrome |
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An amino acid metabolic disorder that is character..[+]
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1 articles | |
cerebral creatine deficiency syndrome 1 |
A cerebral creatine deficiency syndrome that is ch..[+]
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1 articles | ||
congenital adrenal hyperplasia |
congenital lipoid adrenal hyperplasia; adrenal hyp..
[+]
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A steroid inherited metabolic disorder that is cha..[+]
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CHARGE syndrome |
CHARGE association
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A syndrome that is characterized by a pattern of c..[+]
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11 articles | |
cervical dystonia |
spasmodic torticollis
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A focal dystonia that is characterized by simultan..[+]
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cranio-facial dystonia |
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A focal dystonia that is characterized as dystonia..[+]
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1 articles |
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