User:Omer476/Books/List Of Diseases(C)
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List Of Diseases(C)
[edit]- List of diseases (C)
- Trigonocephaly
- Angioedema
- Medullary sponge kidney
- Café au lait spot
- Caffeine-induced sleep disorder
- Infantile cortical hyperostosis
- Calcinosis cutis
- CREST syndrome
- Calciphylaxis
- Calculus (medicine)
- CAMFAK syndrome
- Campylobacteriosis
- Camurati–Engelmann disease
- Canavan disease
- Cancer
- Canga's bead symptom
- Canine distemper
- Cannabis dependence
- Effects of cannabis
- Caplan's syndrome
- Ornithine translocase deficiency
- Carcinoid syndrome
- Squamous-cell carcinoma
- Cardiac amyloidosis
- Cardiac arrest
- Cardiac tamponade
- Cardiofaciocutaneous syndrome
- Cardiomyopathy
- Arrhythmogenic right ventricular dysplasia
- Dilated cardiomyopathy
- Hypertrophic cardiomyopathy
- Restrictive cardiomyopathy
- Achalasia
- Caregiver stress
- Carney complex
- Systemic primary carnitine deficiency
- Carnitine palmitoyltransferase I deficiency
- Carnitine palmitoyltransferase II deficiency
- Carnitine-acylcarnitine translocase deficiency
- Carnosinemia
- Caroli disease
- Carotenosis
- Carotid artery dissection
- Carpal tunnel syndrome
- Carpenter syndrome
- Eosinophilic pneumonia
- Cartilage–hair hypoplasia
- Castleman's disease
- Cri du chat
- Cat eye syndrome
- Cat-scratch disease
- Cataract
- Congenital cataract
- DiGeorge syndrome
- Catel–Manzke syndrome
- Caudal regression syndrome
- Complex regional pain syndrome
- Cavernous hemangioma
- Lymphangioma
- Cavernous sinus thrombosis
- Asymmetric crying facies
- Ondine's curse
- Congenital disorder of glycosylation
- Gluten-sensitive enteropathy-associated conditions
- Coeliac disease
- Cenani–Lenz syndactylism
- Central core disease
- Neurogenic diabetes insipidus
- Central serous retinopathy
- Centronuclear myopathy
- Farber disease
- Fabry disease
- Astraphobia
- Cerebellar agenesis
- Cerebellar hypoplasia
- Cerebral amyloid angiopathy
- Intracranial aneurysm
- CADASIL syndrome
- Sotos syndrome
- Cerebral hypoxia
- Cerebral palsy
- Thrombus
- Ventricular system
- Pashayan syndrome
- Cockayne syndrome
- Neuronal ceroid lipofuscinosis
- Cervical cancer
- Cervical spinal stenosis
- Klippel–Feil syndrome
- Chagas disease
- Chalazion
- Neutral lipid storage disease
- Chancroid
- Iridocorneal endothelial syndrome
- Bardet–Biedl syndrome
- Tachycardia
- Charcot disease
- Charcot–Marie–Tooth disease
- CHARGE syndrome
- Fahr's syndrome
- Chédiak–Higashi syndrome
- Cheilitis
- Paraganglioma
- Chemophobia
- Ho–Kaufman–Mcalister syndrome
- Cherubism
- Arnold–Chiari malformation
- Hyperprolactinaemia
- Chickenpox
- Chikungunya
- CHILD syndrome
- Childhood disintegrative disorder
- Psoriasis
- Chimera (genetics)
- Glutamate flavoring
- Chlamydia trachomatis
- Chlamydia infection
- Chlamydophila pneumoniae
- Cholangiocarcinoma
- Primary sclerosing cholangitis
- Cholecystitis
- Gallstone
- Cholemia
- Cholera
- Progressive familial intrahepatic cholestasis
- Cholestasis
- Cholesteryl ester storage disease
- Lipid pneumonia
- Chondroblastoma
- Chondrocalcinosis
- Chondrodysplasia punctata
- X-linked recessive chondrodysplasia punctata
- Chondrodystrophy
- Ellis–van Creveld syndrome
- Chondroma
- Chondromalacia patellae
- Chondrosarcoma
- Chordoma
- Chorea acanthocytosis
- Sydenham's chorea
- Chorea
- Paroxysmal nonkinesigenic dyskinesia
- Choriocarcinoma
- Chorioretinitis
- Choroid plexus cyst
- Choroid plexus papilloma
- Choroideremia
- Adducted thumb syndrome
- Haemophilia B
- Chromhidrosis
- Chromoblastomycosis
- Renal cell carcinoma
- Trisomy
- 1p36 deletion syndrome
- Chromosome 15q partial deletion
- Chromosome 15q trisomy
- Trisomy 16
- Ring 18
- Edwards syndrome
- 2q37 monosomy
- Ring chromosome 20 syndrome
- Trisomy 22
- Trisomy 8
- Trisomy 9
- Berylliosis
- Chronic obstructive pulmonary disease
- Peptic ulcer
- Chronic fatigue syndrome
- Chronic granulomatous disease
- Hiccup
- Chronic inflammatory demyelinating polyneuropathy
- B-cell chronic lymphocytic leukemia
- Chronic mountain sickness
- Chronic myelogenous leukemia
- Chronic myelomonocytic leukemia
- Vasculitis
- Neutropenia
- Polyradiculoneuropathy
- Chronic recurrent multifocal osteomyelitis
- Chronic kidney disease
- Spasmodic dysphonia
- Neonatal onset multisystem inflammatory disease
- Churg–Strauss syndrome
- Ascites
- Cicatricial pemphigoid
- Ciguatera
- Cinchonism
- Citrullinemia
- Capillary leak syndrome
- Cleft lip and palate
- Cleidocranial dysostosis
- Cloacal exstrophy
- Clouston's hidrotic ectodermal dysplasia
- Club foot
- Cluster headache
- Cytomegalovirus
- Coalworker's pneumoconiosis
- Coats' disease
- Cocaine dependence
- Cocaine intoxication
- Coccidioidomycosis
- Coffin–Lowry syndrome
- Coffin–Siris syndrome
- Cogan syndrome
- Cohen syndrome
- Cold agglutinin disease
- Cold antibody hemolytic anemia
- Urticaria
- Cold urticaria
- Osteogenesis imperfecta
- Colitis
- Connective tissue disease
- Collagenous colitis
- Coloboma
- Hereditary nonpolyposis colorectal cancer
- Intestinal atresia
- Malakoplakia
- Color blindness
- Colorado tick fever
- Combined hyperlipidemia
- Common cold
- Common variable immunodeficiency
- Compartment syndrome
- Complement component 2
- Atrioventricular septal defect
- Conduct disorder
- Conductive hearing loss
- Genital wart
- Condylomata lata
- Cone dystrophy
- Congenital adrenal hyperplasia
- Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
- Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency
- Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
- Lipoid congenital adrenal hyperplasia
- Congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency
- Congenital afibrinogenemia
- Congenital amputation
- Antithrombin
- Amniotic band constriction
- Congenital contractural arachnodactyly
- Congenital pulmonary airway malformation
- Hearing loss
- Congenital diaphragmatic hernia
- Congenital dyserythropoietic anemia
- Gunther disease
- Möbius syndrome
- Congenital fiber type disproportion
- Infantile myofibromatosis
- Megaureter
- Congenital heart defect
- Congenital hemolytic anemia
- Congenital hepatic fibrosis
- Herpes simplex virus
- Congenital hypothyroidism
- Ichthyosis
- Congenital ichthyosiform erythroderma
- Congenital insensitivity to pain with anhidrosis
- Hirschsprung's disease
- Mesoblastic nephroma
- Microvillous inclusion disease
- Mitral valve stenosis
- Mumps
- Congenital myopathy
- Congenital nephrotic syndrome
- Congenital rubella syndrome
- Hereditary spherocytosis
- Congenital syphilis
- Toxoplasmosis
- Heart failure
- Conjunctivitis
- GJB2
- Primary aldosteronism
- Conradi–Hünermann syndrome
- Constitutional growth delay
- Bronchiolitis obliterans
- Contact dermatitis
- Allergic contact dermatitis
- Irritant contact dermatitis
- Conversion disorder
- Cooks syndrome
- Thalassemia
- Menkes disease
- Porphyria
- Pulmonary heart disease
- Cor triatriatum
- Corneal dystrophy
- Cornelia de Lange Syndrome
- Corneodermatoosseous syndrome
- Coronary artery aneurysm
- Coronary artery disease
- Agenesis of the corpus callosum
- Cortical dysplasia
- Corticobasal degeneration
- Costello syndrome
- Costochondritis
- Tietze syndrome
- Robinow syndrome
- Cystic hygroma
- Cowden syndrome
- Cowpox
- Cramp
- Cramp fasciculation syndrome
- Crandall syndrome
- Craniodiaphyseal dysplasia
- Crouzon syndrome
- Craniofrontonasal dysplasia
- Craniosynostosis
- Creatine
- Spirurida
- Cretinism
- Crigler–Najjar syndrome
- CRLF1
- Crohn's disease
- Crome syndrome
- Cronkhite–Canada syndrome
- Croup
- Crouzonodermoskeletal syndrome
- POEMS syndrome
- Cryoglobulinemia
- Cryptococcosis
- Cryptosporidiosis
- Crystal arthropathy
- Currarino syndrome
- Cushing's syndrome
- Anthrax
- Cutaneous larva migrans
- Lupus erythematosus
- Cutaneous T cell lymphoma
- Cutaneous small-vessel vasculitis
- Cutis laxa
- De Barsy syndrome
- Cutis marmorata telangiectatica congenita
- Cutis verticis gyrata
- Cyanide poisoning
- Cyclic neutropenia
- Cyclic vomiting syndrome
- Cyclosporiasis
- Cyclothymia
- Cystic fibrosis
- Cystinosis
- Cystinuria
- Cytochrome c oxidase