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C Syndrome
C3 Glomerulopathy
CACH Syndrome
CAPOS Syndrome
CDKL5 Deficiency Disorder
CHST3-Related Skeletal Dysplasia
CLN1 Disease
CLN2 Disease
CLN3 Disease
CLN4 Disease
CMV Retinitis
COVID-19
Cafe-Au-Lait Spots
Caffey Disease
Calciphylaxis
Calcium Pyrophosphate Arthritis
Calvarial Hyperostosis
Campomelia Cumming Type
Campomelic Dysplasia
Camptocormism
Camptodactyly Fibrous Tissue Hyperplasia Skeletal Dysplasia
Camptodactyly Syndrome Guadalajara Type 1
Camptodactyly Syndrome Guadalajara Type 2
Camptodactyly Taurinuria
Campylobacter Infection
Camurati-Engelmann Disease
Canavan Disease
Candida Infection of the Skin
Canker Sore
Cantu Syndrome
Caput Succedaneum
Carbamoyl Phosphate Synthetase 1 Deficiency
Carbuncle
Carcinoid Syndrome
Carcinoma of the Vocal Tract
Cardiac Amyloidosis
Cardiac Arrest
Cardiac Diverticulum
Cardiac Tamponade
Cardiofaciocutaneous Syndrome
Cardiogenic Shock
Cardiomyopathic Lentiginosis
Cardiomyopathy
Cardiomyopathy Due to Anthracyclines
Cardiomyopathy Hypogonadism Metabolic Anomalies
Cardiospasm
Carey-Fineman-Ziter Syndrome
Carney Complex
Carnitine Palmitoyltransferase 1 Deficiency
Carnitine-Acylcarnitine Translocase Deficiency
Caroli Disease
Carpal Tunnel Syndrome
Carpenter Syndrome
Cartilage-Hair Hypoplasia
Castleman Disease
Cat Eye Syndrome
Cat Scratch Disease
Cataract
Cataract Ataxia Deafness
Catecholaminergic Polymorphic Ventricular Tachycardia
Caudal Appendage Deafness
Caudal Duplication
Caudal Regression Syndrome
Cavernous Lymphangioma
Cavernous Sinus Thrombosis
Celiac Disease
Cellulitis
Central Core Disease
Central Pain Syndrome
Central Serous Chorioretinopathy
Central Sleep Apnea
Centronuclear Myopathy
Cerebellar Agenesis
Cerebellar Degeneration
Cerebellar Hypoplasia
Cerebellar Multiple System Atrophy
Cerebelloolivary Atrophy
Cerebelloparenchymal Disorder 3
Cerebellum Agenesis Hydrocephaly
Cerebral Amyloid Angiopathy
Cerebral Arteriovenous Malformation
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
Cerebral Cavernous Malformation
Cerebral Hypoxia
Cerebral Palsy
Cerebral Ventricle Cancer
Cerebrospinal Fluid Leak
Cerebrotendinous Xanthomatosis
Cervical Cancer
Cervical Dysplasia
Cervical Polyps
Cervical Spondylosis
Cervicitis
Chagas Disease
Chalazion
Chanarin-Dorfman Syndrome
Chancroid
Chandler's Syndrome
Chaotic Atrial Tachycardia
Char Syndrome
Charcot-Marie-Tooth Disease
Charles Bonnet Syndrome
Charlie M Syndrome
Chediak-Higashi Syndrome
Cheilitis Glandularis
Chemical Pneumonitis
Chemosis
Cherry Angioma
Cherubism
Chiari Malformation
Chiari Malformation Type 1
Chiari Malformation Type 2
Chickenpox
Chikungunya
Childhood Acute Myeloid Leukemia
Childhood Disintegrative Disorder
Childhood Hypophosphatasia
Childhood Iron Deficiency Anemia
Childhood Pancreatitis
Childhood Volvulus
Chinese Restaurant Syndrome
Chlamydia
Choanal Atresia
Cholangiocarcinoma
Cholangitis
Cholecystitis
Choledocholithiasis
Cholera
Cholestasis
Cholesteatoma
Cholesterol Pneumonia
Cholesteryl Ester Storage Disease
Chondroblastoma
Chondrocalcinosis 2
Chondrodysplasia Punctata Syndrome
Chondrodysplasia Punctata with Steroid Sulfatase Deficiency
Chondrodysplasia, Grebe Type
Chondrodystrophy
Chondroma
Chondrosarcoma
Chordoma
Chorea
Chorea-Acanthocytosis
Choriocarcinoma
Choroid Plexus Carcinoma
Choroid Plexus Cyst
Choroid Plexus Papilloma
Choroideremia
Chromoblastomycosis
Chromophobe Renal Cell Carcinoma
Chromosome 10q Deletion
Chromosome 11 Uniparental Disomy
Chromosome 11q Duplication
Chromosome 12p Deletion
Chromosome 12p Duplication
Chromosome 13q Deletion
Chromosome 13q Duplication
Chromosome 15q Deletion
Chromosome 15q Duplication
Chromosome 16 Trisomy
Chromosome 16q Duplication
Chromosome 18p Deletion
Chromosome 18q Duplication
Chromosome 2 Uniparental Disomy
Chromosome 20 Trisomy
Chromosome 21q Deletion
Chromosome 22 Duplication
Chromosome 2p Duplication
Chromosome 3q Duplication
Chromosome 4p Deletion
Chromosome 4q Deletion
Chromosome 4q Duplication
Chromosome 5q Duplication
Chromosome 6 Uniparental Disomy
Chromosome 6p Duplication
Chromosome 6q Deletion
Chromosome 6q Duplication
Chromosome 7p Deletion
Chromosome 7p Duplication
Chromosome 7q Duplication
Chromosome 8p Deletion
Chromosome 9p Deletion
Chronic Antibody-Mediated Rejection
Chronic B-Cell Leukemia
Chronic Cough
Chronic Demyelinizing Neuropathy with IgM Monoclonal
Chronic Eosinophilic Pneumonia
Chronic Erosive Gastritis
Chronic Fatigue Syndrome
Chronic Granulomatous Disease
Chronic Inflammatory Demyelinating Polyneuropathy
Chronic Kidney Disease
Chronic Lymphocytic Leukemia
Chronic Myelogenous Leukemia
Chronic Myelomonocytic Leukemia
Chronic Obstructive Pulmonary Disease
Chronic Pancreatitis
Chronic Polyradiculoneuritis
Chronic Recurrent Multifocal Osteomyelitis
Chronic Subdural Hematoma
Chronic T-Cell Leukemia
Chylous Ascites
Cicatricial Pemphigoid
Ciliary Dyskinesia-Bronchiectasis
Circumferential Skin Creases Kunze Type
Cirrhosis
Citrullinemia
Classic Galactosemia
Claw Foot
Cleft Hand Absent Tibia
Cleft Lip and Palate
Cleft Tongue
Cleidocranial Dysplasia
Cln5 Disease
Cloacal Exstrophy
Cloudy Cornea
Clouston Syndrome
Clubbing of the Fingers or Toes
Clubfoot
Cluster Headache
Coach Syndrome
Coal Worker's Pneumoconiosis
Coarctation of the Aorta
Coats Disease
Coccidioidomycosis
Cockayne Syndrome
Cockayne Syndrome Type 1
Cockayne Syndrome Type 2
Coenzyme Q Cytochrome C Reductase Deficiency
Coffin-Lowry Syndrome
Coffin-Siris Syndrome
Cogan's Syndrome
Cogan-Reese Syndrome
Cohen Syndrome
Cold Urticaria
Cold-Induced Sweating Syndrome
Colitis
Collagenous Colitis
Collapsed Lung
Collins Pope Syndrome
Coloboma
Coloboma of Eye Lens
Coloboma of Iris
Coloboma of Optic Nerve
Coloboma of Optic Papilla
Colonic Atresia
Colonic Malakoplakia
Color Blindness
Colorado Tick Fever
Colorectal Cancer
Comedones
Common Cold
Common Peroneal Nerve Dysfunction
Common Variable Immune Deficiency
Compartment Syndrome
Complement Component 2 Deficiency
Complex Regional Pain Syndrome
Concussion
Cone Dystrophy
Cone Rod Dystrophy Amelogenesis Imperfecta
Cone-Rod Dystrophy
Congenital Adrenal Hyperplasia
Congenital Afibrinogenemia
Congenital Aneurysms of the Great Vessels
Congenital Anti-Plasmin Deficiency
Congenital Antithrombin 3 Deficiency
Congenital Aplastic Anemia
Congenital Arteriovenous Shunt
Congenital Bilateral Absence of the Vas Deferens
Congenital Bronchobiliary Fistula
Congenital Cardiovascular Shunt
Congenital Cataract
Congenital Central Hypoventilation Syndrome
Congenital Contractural Arachnodactyly
Congenital Contractures
Congenital Cytomegalovirus
Congenital Diaphragmatic Hernia
Congenital Erythropoietic Porphyria
Congenital Femoral Deficiency
Congenital Fiber-Type Disproportion
Congenital Generalized Fibromatosis
Congenital Generalized Lipodystrophy
Congenital Giant Megaureter
Congenital Heart Block
Congenital Heart Disease
Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limbs Defects
Congenital Hemolytic Anemia
Congenital Hepatic Fibrosis
Congenital Herpes Simplex
Congenital Hyperinsulinism
Congenital Hypothyroidism
Congenital Hypotrichosis Milia
Congenital Insensitivity to Pain with Anhidrosis
Congenital Lipoid Adrenal Hyperplasia
Congenital Lobar Emphysema
Congenital Mesoblastic Nephroma
Congenital Microcoria
Congenital Mirror Movement Disorder
Congenital Mitral Malformation
Congenital Mitral Stenosis
Congenital Mumps
Congenital Muscular Dystrophy Type 1A
Congenital Myasthenic Syndrome
Congenital Nephrotic Syndrome
Congenital Nonhemolytic Jaundice
Congenital Plasminogen Deficiency
Congenital Pulmonary Lymphangiectasia
Congenital Radioulnar Synostosis
Congenital Sucrase-Isomaltase Deficiency
Congenital Syphilis
Congenital Toxoplasmosis
Congenital Tracheomalacia
Congenital Unilateral Pulmonary Hypoplasia
Conjunctivitis
Conjunctivitis with Pseudomembrane
Constrictive Pericarditis
Contact Dermatitis
Continuous Muscle Fiber Activity Hereditary
Continuous Spike-Wave During Slow Sleep Syndrome
Contracture Deformity
Conversion Disorder
Cor Pulmonale
Cor Triatriatum
Corneal Dystrophy and Perceptive Deafness
Cornelia De Lange Syndrome
Corns and Calluses
Coronary Arteries Congenital Malformation
Coronary Artery Aneurysm
Coronary Artery Fistula
Coronary Artery Spasm
Coronary Heart Disease
Corpus Callosum Agenesis
Corpus Callosum Dysgenesis Hypopituitarism
Cortical Dysplasia
Corticobasal Degeneration
Costello Syndrome
Cowden Syndrome
Cramp-Fasciculation Syndrome
Cranio Osteoarthropathy
Craniodiaphyseal Dysplasia
Cranioectodermal Dysplasia
Craniofacial-Deafness-Hand Syndrome
Craniofrontonasal Dysplasia
Craniometaphyseal Dysplasia
Craniopharyngioma
Craniosynostosis
Craniosynostosis Autosomal Dominant
Craniotabes
Creeping Eruption
Creutzfeldt-Jakob Disease
Cri-Du-Chat Syndrome
Crigler-Najjar Syndrome
Crohn's Disease
Cronkhite-Canada Disease
Croup
Crouzon Syndrome
Cryoglobulinemia
Cryptococcal Meningitis
Cryptococcosis
Cryptosporidium Enteritis
Culler Jones Syndrome
Currarino Triad
Curry Jones Syndrome
Cushing Syndrome
Cushing Syndrome due to Adrenal Tumor
Cutaneous Lupus Erythematosus
Cutaneous T-Cell Lymphoma
Cutis Gyrata Syndrome
Cutis Laxa
Cutis Laxa, Autosomal Recessive Type 1
Cutis Marmorata Telangiectatica Congenita
Cyclic Neutropenia
Cyclic Vomiting Syndrome
Cyclothymic Disorder
Cystic Adenomatoid Malformation of Lung
Cystic Fibrosis
Cystic Hygroma
Cystic Medial Necrosis of Aorta
Cysticercosis
Cystinosis
Cystinuria
Cystoisosporiasis
Cytochrome C Oxidase Deficiency
Cytochrome P450 Oxidoreductase Deficiency
Cytomegalic Inclusion Disease
Cytomegalovirus Antenatal Infection
Cytomegalovirus Infection
Cytoplasmic Body Myopathy
