C Diseases
From Anvita Health Wiki
Introduction
- C syndrome
- C-like syndrome
- C1q deficiency
- C6, C7 radiculopathy
- cabezas x linked mental retardation syndrome
- cachexia
- cachexia-anorexia syndrome
- CADASIL
- cadmiun toxicity
- cafe au lait spot
- Caffey's disease
- Caisson disease
- calcific tendonitis
- calcifying epithelioma of Malherbe
- calcinosis
- calciphylaxis
- calcium pyrophosphate dihydrate crystal deposition
- calcium stone
- calf pain
- callus
- Campbell de Morgan spot
- campomelic dysplasia
- camptodactyly tall stature & hearing loss syndrome
- camptodactyly-arthropathy-coxa vara-pericarditis syndrome
- Canavan-van Bogaert-Bertrand spongy degeneration
- cancer
- cancer family syndrome
- cancer of the lung
- cancer pain
- cancer-associated retinopathy syndrome
- cancrum oris novum
- Candida vulvovaginosis
- candidemia
- candidiasis
- candidiasis hypersensitivity syndrome
- candiduria
- canker sore
- capillary hemangioma of infancy
- capillary malformation-arteriovenous malformation
- Caplan's syndrome
- caput medusae
- carbamate toxicity
- carbamoyl phosphate synthetase deficiency
- carbohydrate-deficient glycoprotein syndrome type 1A
- carbohydrate-deficient glycoprotein syndrome type 1B
- carbohydrate-deficient glycoprotein syndrome type 2
- carbohydrate-deficient glycoprotein syndrome type 4
- carbon monoxide poisoning
- carbuncle
- carcininoma, adrenal cortex
- carcinoid
- carcinoid syndrome
- carcinoma
- carcinoma in situ
- carcinoma of the breast
- carcinoma of the colon
- carcinoma of the lung
- carcinoma of the ovary
- carcinoma of the thymus
- carcinomatous meningitis
- carcinosarcoma
- cardiac amyloidosis
- cardiac angina
- cardiac arrest
- cardiac arrhythmia
- cardiac device infection
- cardiac embolism
- cardiac murmur
- cardiac myxoma
- cardiac neoplasm
- cardiac tamponade
- cardiac transplantation
- cardioembolic
- cardioembolism
- cardiofaciocutaneous syndrome
- cardiogenic pulmonary edema
- cardiogenic shock
- cardiomegaly
- cardiomyopathy
- cardiomyopathy hypertrophic with mid-left ventricular chamber type 1
- cardiotoxicity
- cardiovascular disease
- cardiovascular disease in women
- caregiver stress
- Carney complex
- Carney complex 1
- Carney complex 2
- Carney triad
- carnitine deficiency
- carnitine palmitoyltransferase 1 deficiency
- carnitine palmitoyltransferase 2 deficiency
- carnitine palmitoyltransferase deficiency
- carnitine-acylcarnitine translocase deficiency
- carotenemia
- carotenodermia
- carotid artery dissection
- carotid artery stenosis
- carotid body tumor
- carotid bruit
- carotid sinus syndrome
- carotid stenosis
- carotid-cavernous fistula
- carpal tunnel syndrome
- Carpenter syndrome
- Carpenter-Waziri syndrome
- carpopedal spasm
- cartilage fibrillation
- Carvajal syndrome
- caspase-8 deficiency
- Castleman lymphadenopathy
- cat scratch disease
- cat-eye syndrome
- catalepsy
- cataplexy
- cataract posterior polar type 4
- cataracts
- catatonia
- catatonic schizophrenia
- CATCH22 syndrome
- catecholaminergic polymorphic ventricular tachycardia
- catheter-associated urinary tract infection
- cauda equina syndrome
- caudal duplication anomaly
- causalgia
- causes of acute pancreatitis
- cavernous hemangioma
- cavernous sinus syndrome
- cavernous sinus thrombosis
- CD36 deficiency
- cecitis
- CEDNIK syndrome
- celiac sprue
- cell-mediated hypersensitivity
- cellophane maculopathy
- cellular immune dysfunction
- cellulitis
- central adrenal insufficiency
- central areolar choroidal dystrophy
- central cord syndrome
- central core disease of muscle
- central deafness
- central diabetes insipidus
- central hearing loss
- central hypoventilation syndrome
- central nervous system neoplasm
- central neurocytoma
- central pain syndrome
- central pontine myelinolysis
- central precocious puberty
- central sleep apnea
- central vertigo
- cephalopelvic disproportion
- cerebellar ataxia
- cerebellar ataxia early-onset with apraxia & hypoalbuminemia
- cerebellar ataxia, Cayman-type
- cerebellar degeneration
- cerebellar dysmetria
- cerebellar infarction
- cerebellar signs
- cerebellar tremor
- cerebello-oculo-renal syndrome
- cerebral amyloid angiopathy
- cerebral amyloid angiopathy ITM2B-related type 1
- cerebral amyloid angiopathy ITM2B-related type 2
- cerebral amyloid microangiopathy
- cerebral aneurysm
- cerebral arteriovenous malformation
- cerebral autosomal dominant arteriopathy with subcortical infarcts & leukoencephalopathy
- cerebral cavernous malformation
- cerebral concussion
- cerebral cortical dysplasia
- cerebral gigantism
- cerebral granulomatous angiitis
- cerebral hemorrhage
- cerebral ischemia
- cerebral malaria
- cerebral palsy
- cerebral palsy spastic quadriplegic type 2
- cerebro-oculo-facio-skeletal syndrome
- cerebrofrontofacial syndrome
- cerebrohepatorenal syndrome
- cerebroocular dysplasia-muscular dystrophy syndrome
- cerebroretinal vasculopathy
- cerebrospinal fluid leakage
- cerebrospinal fluid rhinorrhea
- cerebrotendinous xanthomatosis
- cerebrovascular disease
- ceroid lipofuscinosis
- cerumen impactation
- cervical cancer
- cervical dystonia
- cervical erosion
- cervical incompetence
- cervical intraepithelial neoplasia
- cervical motion tenderness
- cervical rib
- cervical rib & band syndrome
- cervical rib syndrome
- cervical spinal stenosis
- cervical spine fracture
- cervical spine injury
- cervical venous hum
- cervicitis
- CETP deficiency
- chafing
- chagoma
- chalazion
- chancroid
- chandelier sign
- Char syndrome
- Charcot joint
- charcot marie tooth disease dominant intermediate b
- charcot marie tooth disease dominant intermediate c
- charcot marie tooth disease type 4a
- charcot marie tooth disease type 4b1
- charcot marie tooth disease type 4b2
- charcot marie tooth disease type 4c
- charcot marie tooth disease type 4e
- charcot marie tooth disease type 4f
- Charcot's syndrome
- Charcot's triad
- Charcot-Marie-Tooth disease
- Charcot-Marie-Tooth disease dominant intermediate D
- Charcot-Marie-Tooth disease type 1
- Charcot-Marie-Tooth disease type 1A
- Charcot-Marie-Tooth disease type 1D
- Charcot-Marie-Tooth disease type 1E
- Charcot-Marie-Tooth disease type 1F
- Charcot-Marie-Tooth disease type 2
- Charcot-Marie-Tooth disease type 2A1
- Charcot-Marie-Tooth disease type 2A2
- Charcot-Marie-Tooth disease type 2B
- Charcot-Marie-Tooth disease type 2D
- Charcot-Marie-Tooth disease type 2G
- Charcot-Marie-Tooth disease type 2I
- Charcot-Marie-Tooth disease type 2J
- Charcot-Marie-Tooth disease type 2K
- Charcot-Marie-Tooth disease type-5
- CHARGE syndrome
- Charles Bonnet syndrome
- Chediak-Higashi syndrome
- cheilitis
- cheilitis glandularis
- cheilodynia (lip pain)
- cheiroarthropathy
- chemical leukoderma
- chemical pneumonitis
- Chemke syndrome
- cherry angioma
- cherry red spot-myoclonus syndrome
- cherubism
- chest pain
- chest pain syndrome
- Cheyne-Stokes respiration
- Chiari malformation
- Chiari-Frommel syndrome
- chickenpox
- chilblain lupus erythematosus
- child abuse
- CHILD syndrome
- childhood absence epilepsy type 2
- childhood absence epilepsy type 3
- childhood absence epilepsy type 4
- childhood disease
- childhood exanthum
- childhood infection
- childhood polycystic kidney disease
- childhood spinal muscular atrophy
- chills
- chloasma
- chloracne
- chloroma
- choanal atresia
- cholangiocarcinoma
- cholangitis
- cholangitis lenta
- cholecystitis
- choledochal cyst
- choledocholithiasis
- cholelithiasis
- cholera
- cholestasis
- cholestasis with delta(4)-3-oxosteroid 5-beta-reductase deficiency
- cholestatic hepatitis
- cholesteatoma
- cholesteryl ester transfer protein deficiency
- chondroblastoma
- chondrocalcinosis
- chondrodermatitis nodularis
- chondrodermatitis nodularis chronica helicis
- chondrodysplasia
- chondrodysplasia punctata
- chondrodysplasia punctata 1, X-linked recessive
- chondrodysplasia punctata X-linked dominant type 2
- chondrodysplasia punctata-2
- chondrodystrophy
- chondroectodermal dysplasia
- chondrolysis
- chondroma
- chondrosarcoma
- chordoid glioma
- chordoma
- chorea
- choreoacanthyocytosis
- chorioamnionitis
- choriocarcinoma
- chorioretinitis
- choroid plexus papilloma
- choroidal detachment
- choroidal neovascular membrane
- choroideremia
- choroiditis
- Christ-Siemens-Touraine syndrome
- Christmas disease
- chromatopsia
- chromium deficiency
- chromium toxicity
- chromoblastomycosis
- chromophobe renal cell carcinoma
- chromosomal 5p deletion syndrome
- chromosome 10q23 deletion syndrome
- chromosome 22q13.3 deletion syndrome
- chromosome 9q subtelomeric deletion syndrome
- chronic abdominal pain
- chronic active hepatitis
- chronic bronchitis
- chronic bullous disease of childhood
- chronic cerebrospinal venous insufficiency
- chronic childhood spinal muscular atrophy
- chronic cicatrizing enteritis
- chronic congenital idiopathic hyperphosphatasia
- chronic cough
- chronic cutaneous lupus erythematosus
- chronic daily headache
- chronic diarrhea
- chronic eosinophilic pneumonia
- chronic fatigue syndrome
- chronic granulomatous disease
- chronic heart failure
- chronic hepatitis
- chronic hypercapneic respiratory failure
- chronic hyperplastic sinusitis
- chronic hypersensitivity pneumonitis
- chronic hypertension
- chronic idiopathic ataxic neuropathy
- chronic idiopathic intestinal pseudo-obstruction
- chronic idiopathic jaundice
- chronic infantile neurologic cutaneous articular syndrome
- chronic inflammatory demyelinating polyradiculoneuropathy
- chronic interstitial nephritis
- chronic kidney failure
- chronic leukemia
- chronic lymphatic leukemia type 2
- chronic lymphocytic leukemia
- chronic lymphocytic thyroiditis
- chronic mitral regurgitation
- chronic mountain sickness
- chronic mucocutaneous candidiasis
- chronic musculoskeletal pain
- chronic myeloid leukemia
- chronic myeloid leukemia/philadelphia chromosome
- chronic myelomonocytic leukemia
- chronic myeloproliferative disorder
- chronic non-spherocytic hemolytic anemia
- chronic obstructive pulmonary disease
- chronic pain
- chronic pancreatitis
- chronic pelvic pain syndrome
- chronic pulmonary fibrosis
- chronic pyelonephritis
- chronic renal failure
- chronic serous otitis media
- chronic simple silicosis
- chronic sinusitis
- chronic suppurative otitis media
- chronic traumatic encephalopathy
- Churg-Strauss disease
- Chuvash type polycythemia
- chylomicron retention disease
- chylous pleural effusion
- chyluria
- cicatricial pemphigoid
- cicatrizing perifolliculitis
- cigarette smoking
- ciliary disorder
- ciliary dyskinesia
- cinchonism
- cirrhosis
- cirsocele
- citrullinemia
- citrullinemia type 1
- citrullinemia type 2
- citrullinuria
- CK syndrome
- Clark's melanocytic nevus
- classic Bartter syndrome
- classic cervical rib syndrome
- classic lissencephaly
- claudication
- clavus
- claw foot
- clear cell carcinoma
- clear cell sarcoma
- cleft lip
- cleft palate
- cleidocranial dysplasia
- cleidocranial dysplasia with parietal foramina
- clinical dehydration
- CLL (chronic lymphocytic leukemia)
- clonorchiasis
- clonus
- closed-angle glaucoma
- Clostridium difficile-associated diarrhea
- Cloud 9
- clubbed fingers
- clubbing
- clubfoot
- cluster A personality disorder
- cluster B personality disorder
- cluster C personality disorder
- cluster headache
- CML (chronic myeloid leukemia)
- cml blast crisis
- CMML (chronic myelomonocytic leukemia)
- CMT5
- CMV
- CMV pneumonitis
- CMV retinitis
- coagulation disorder
- coagulation factor V deficiency
- coagulation factor VII deficiency
- coagulation factor VIII deficiency
- coagulation factor X deficiency
- coagulation factor XI deficiency
- coagulation factor XII deficiency
- coarctation of aorta
- Cobb's syndrome
- cocaine abuse
- coccidioidomycosis
- coccygodynia
- Cochin Jewish disorder
- Cockayne syndrome
- Cockayne syndrome type 2
- coenurosis
- coenzyme Q10 deficiency
- Coffin-Lowry syndrome
- Cogan's syndrome
- cognitive impairment
- cognitive impairment in the elderly
- coin ingestion
- coinfection
- cold agglutinin syndrome
- cold hemoglobinuria
- cold induced sweating syndrome
- cold sore
- cold-stimulus headache
- collagenous colitis
- collagenous fibroma
- Colles' fracture
- colloid goiter
- collum distortum
- coloboma
- colon obstruction
- colonic aganglionosis
- colonic pseudo-obstruction
- colonic ulceration
- color vision impairment
- colorblindness
- colorectal adenocarcinoma
- colorectal adenomatous polyp
- colorectal polyp
- colovesicle fistula
- coma
- comatose
- combined immune deficiency
- combined oxidative phosphorylation deficiency
- combined oxidative phosphorylation deficiency type 3
- combined oxidative phosphorylation deficiency type 4
- combined oxidative phosphorylation deficiency type 8
- combined pituitary hormone deficiency
- common bile duct stone
- common cold
- common variable immunodeficiency
- common wart
- community-acquired pneumonia
- comorbid conditions that increase mortality of upper GI bleed
- compartment syndrome
- competitive atrioventricular dissociation
- complement deficiency
- complete heart block
- complex 1 mitochondrial respiratory chain deficiency
- complex partial seizure
- complex regional pain syndrome type 1
- complex regional pain syndrome type 2
- complex subdural hygroma
- complicated silicosis
- complications of the puerperium
- compound melanocytic nevus
- compression fracture of vertebral column
- Compton-North congenital myopathy
- compulsion
- concha bullosa
- conduction aphasia
- conduction block
- conductive hearing loss
- condyloma acuminata
- condyloma latum
- cone-rod dystrophy
- cone-rod dystrophy type 12
- confusion
- confusional state
- congenital adrenal hyperplasia
- congenital adrenal hypoplasia
- congenital afibrinogenemia
- congenital alcoholism
- congenital alveolar capillary dysplasia
- congenital amegakaryocytic thrombocytopenia
- congenital anomaly
- congenital atrichia
- congenital bilateral absence of the vas deferens
- congenital bile acid synthesis defect type 2
- congenital brachial plexus injury
- congenital cataracts facial dysmorphism & neuropathy syndrome
- congenital central hypoventilation syndrome
- congenital cerulean cataract 4
- congenital chloride diarrhea
- congenital contracture syndrome
- congenital cutaneous neurilemmomatosis
- congenital diaphragmatic hernia
- congenital diarrhea type 2
- congenital diarrhea type 3
- congenital diarrhea type 4
- congenital disorder of glycosylation
- congenital disorder of glycosylation 2b
- congenital disorder of glycosylation 2C
- congenital disorder of glycosylation type 1A
- congenital disorder of glycosylation type 1B
- congenital disorder of glycosylation type 1C
- congenital disorder of glycosylation type 1D
- congenital disorder of glycosylation type 1E
- congenital disorder of glycosylation type 1G
- congenital disorder of glycosylation type 1H
- congenital disorder of glycosylation type 1i
- congenital disorder of glycosylation type 1J
- congenital disorder of glycosylation type 1K
- congenital disorder of glycosylation type 2A
- congenital disorder of glycosylation type 2C
- congenital disorder of glycosylation type 2D
- congenital disorder of glycosylation type 2G
- congenital dyserythropoietic anemia
- congenital dyserythropoietic anemia-1
- congenital dyserythropoietic anemia-2
- congenital dyserythropoietic anemia-3
- congenital erythroid hypoplasia
- congenital erythropoietic porphyria
- congenital facial diplegia
- congenital generalized lipodystrophy type 1
- congenital generalized lipodystrophy type 2
- congenital generalized lipodystrophy type 3
- congenital glucose/galactose malabsorption
- congenital heart defect
- congenital hemidysplasia with ichthyosiform erythroderma & limb defects
- congenital hereditary endothelial dystrophy of cornea
- congenital hyperinsulinism
- congenital hypomyelination neuropathy
- congenital hypoplastic neutropenia
- congenital hypothyroidism
- congenital hypothyroidism due to dyshormonogenesis type 1
- congenital hypothyroidism due to TSH resistance
- congenital hypothyroidism non-goitrous type 1
- congenital hypothyroidism non-goitrous type 2
- congenital ichthyosiform erythroderma
- congenital ichthyosis
- congenital infantile lactic acidosis
- congenital insensitivity to pain with anhidrosis
- congenital lactase deficiency
- congenital lipoid adrenal hyperplasia
- congenital long QT syndrome
- congenital megacolon
- congenital melanocytic nevus
- congenital myasthenic syndrome
- congenital myasthenic syndrome type 1C
- congenital myasthenic syndrome with acetylcholine receptor deficiency
- congenital myopathy due to ITGA7 defect
- congenital myopathy with fiber-type disproportion
- congenital nephrotic syndrome
- congenital nephrotic syndrome of the Finnish type
- congenital neutropenia G6PC3 type
- congenital neutropenia type 3
- congenital nonbullous ichthyosiform erythroderma
- congenital nonlysosomal cardiac glycogenosis
- congenital Ondine curse
- congenital sensorineural deafness X-linked 2
- congenital stationary night blindness
- congenital stationary night blindness 1 X-linked
- congenital stationary night blindness 1B
- congenital stationary night blindness Oguchi type
- congenital stationary night blindness type 1
- congenital stationary night blindness type 2
- congenital stromal corneal dystrophy
- congenital vertical talus
- conjunctival chalasis
- conjunctival melanoma
- conjunctivitis
- Conn's syndrome
- conotruncal heart malformation
- conradi hunermann syndrome
- constipation
- constrictive pericarditis
- contact dermatitis
- contiguous ABCD1/DXS1375E deletion syndrome
- continuous cardiac murmur
- continuous heart murmur
- continuous murmur
- continuous muscle fiber activity syndrome
- contracture
- contrast nephropathy
- contrecoup injury
- contusion
- conversion disorder
- convulsion
- convulsive disorder & mental retardation
- convulsive status epilepticus
- Cooley's anemia
- COPD exacerbation
- copper deficiency
- coprolalia
- cor pulmonale
- Cori-Forbes type glycogen storage disease
- corneal abrasion
- corneal dystrophy & perceptive deafness
- corneal ectasia
- corneal endothelial dystrophy type 2
- corneal epithelial basement membrane dystrophy
- corneal fleck dystrophy
- corneal perforation
- corneal reflex
- corneal ulcer
- Cornelia de Lange syndrome
- Cornelia de Lange syndrome 3
- coronal craniosynostosis, non-syndromic, Muenke type
- coronary artery calcification
- coronary artery disease
- coronary artery thrombosis
- coronary stenosis
- coronary syndrome X
- coronary vasospasm
- corpus callosum agenesis mental retardation ocular coloboma micrognathia
- corpus callosum hypoplasia, psychomotor retardation, adducted thumbs, spastic paraparesis, & hydrocephalus
- cortical dysplasia-focal epilepsy syndrome
- corticobasal degeneration
- corticosterone methyloxidase type 1 deficiency
- cortisone reductase deficiency
- cosmetic disorder
- costa cervicalis
- Costeff optic atrophy syndrome
- Costello syndrome
- costochondritis
- costovertebral angle tenderness
- cough
- cough tic
- cow's milk hypersensitivity
- Cowden's disease
- CPPD disease
- CPS1 deficiency
- cramp
- cranial arteritis
- cranial fracture
- cranial nerve 7 palsy
- cranial nerve III palsy
- cranial nerve palsy
- craniofacial dysostosis type 1
- craniofacial-deafness-hand syndrome
- craniolenticulosutural dysplasia
- craniometaphyseal dysplasia Jackson type
- cranioorodigital syndrome
- cranioosteoarthropathy
- craniopharyngioma
- craniosynostosis
- craniosynostosis 1
- craniosynostosis 2
- craniosynostosis with radial defects
- Cree encephalitis
- cremasteric reflex
- crepitus
- crescentic glomerulonephritis
- CREST syndrome
- cretinism
- Creutzfeldt-Jakob disease
- CRFoma
- cri-du-chat syndrome
- crigler najjar syndrome 1
- crigler najjar syndrome 2
- Criswick-Schepens syndrome
- critical disease
- critical illness polyneuropathy
- critical illness weakness
- Crohn's disease
- Cronkhite-Canada syndrome
- croup
- Crouzon syndrome
- Crow-Fukase syndrome
- crush injury
- crush syndrome
- Cruveilhier-Baumgarten syndrome
- cry of the cat syndrome
- cryofibrinogenemia
- cryoglobulinemia
- cryoglobulinemia, type 1
- cryoglobulinemia, type 2
- cryoglobulinemia, type 3
- cryohydrocytosis
- cryopyrin associated periodic syndrome
- cryptogenic organizing pneumonia
- cryptophthalmos syndrome
- cryptorchidism
- cryptorchism
- cryptosporidiosis
- crystalline arthritis
- cubital tunnel syndrome
- cumulative trauma disorder
- Currarino syndrome
- Curry-Hall syndrome
- Cushing's syndrome
- cutaneous B-cell lymphoma
- cutaneous candidiasis
- cutaneous larva migrans
- cutaneous leishmaniasis
- cutaneous leukocytoclastic vasculitis
- cutaneous melanoma
- cutaneous T-cell lymphoid dyscrasia
- cutaneous T-cell lymphoma
- cutaneous ulcer
- cutis laxa
- cutis laxa type I
- cutis laxa type II
- cutis marmorata
- cyanide poisoning
- cyanosis
- cyclic hematopoiesis
- cyclic ichthyosis with epidermolytic hyperkeratosis
- cyclic neutropenia
- cyclic vomiting syndrome
- cycloplegia
- cyclothymic disorder
- cystadenocarcinoma
- cystadenoma
- cystathioninuria
- cystic fibrosis
- cysticercosis
- cystine stone
- cystinosis
- cystinuria
- cystitis
- cystoid macular edema
- cystosarcoma phyllodes
- cytochrome C oxidase deficiency
- cytomegalovirus
More General Terms
C - diseases