Condition
30,467 condition in the knowledge graph · page 107.
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Candidiasis, Familial, 8
syndrome
disease
Candidiasis, Familial, 9
syndrome
disease
Candidiasis, Vulvovaginal
syndrome
ICD-10 B37.3
disease · Infections; Female Urogenital Diseases and Pregnancy Complications
Cannabis Abuse
disease
disease · Mental Disorders; Chemically-Induced Disorders
Cannabis Dependence
disease
disease · Mental Disorders; Chemically-Induced Disorders
Cannabis Use
disease
disease
Cannabis Withdrawal
disease
disease
Cannabis-Related Disorder
group
group · Mental Disorders; Chemically-Induced Disorders
Cantu Syndrome
syndrome
disease · Cardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
Cap Myopathy
syndrome
disease · Nervous System Diseases; Musculoskeletal Diseases
Cap Myopathy 1
syndrome
disease
Cap Myopathy 2
syndrome
disease
Cap Myopathy, Tpm2-Related
syndrome
disease · Nervous System Diseases; Musculoskeletal Diseases
Cap Myopathy, Tpm3-Related (Disorder)
syndrome
disease · Nervous System Diseases; Musculoskeletal Diseases
Cap Polyposis
disease
disease
Capillariasis
syndrome
disease · Infections
Capillaritis
syndrome
disease · Cardiovascular Diseases; Hemic and Lymphatic Diseases; Pathological Conditions, Signs and Symptoms
Capillary Fragility
syndrome
disease
Capillary Hemangioma of Retina
disease
disease · Cardiovascular Diseases; Neoplasms
Capillary Hyperpermeability
syndrome
disease
Capillary Leak Syndrome
syndrome
disease · Cardiovascular Diseases
Capillary Malformation (Disorder)
disease
disease · Cardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Capillary Malformation Without Arteriovenous Malformation
syndrome
disease · Cardiovascular Diseases; Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Capillary Malformation-Arteriovenous Malformation (Disorder)
syndrome
disease · Cardiovascular Diseases; Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Capillary Malformation-Arteriovenous Malformation 1
syndrome
disease
Capillary Malformation-Arteriovenous Malformation 2
syndrome
disease
Capillary Thrombosis
syndrome
disease · Cardiovascular Diseases
Capillary-Venous Malformation
disease
disease · Cardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Capitate-Hamate Fusion
phenotype
phenotype
Caplan Syndrome
syndrome
disease · Occupational Diseases; Skin and Connective Tissue Diseases; Respiratory Tract Diseases; Musculoskeletal Diseases
Capnocytophaga Canimorsus Sepsis
syndrome
disease
Capos Syndrome
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Eye Diseases; Pathological Conditions, Signs and Symptoms; Otorhinolaryngologic Diseases; Musculoskeletal Diseases
Capsular Cataract (Disorder)
syndrome
disease · Eye Diseases
Carbamoyl Phosphate Synthase 1 Deficiency
syndrome
disease · Nervous System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Carbamoyl-Phosphate Synthase I Deficiency Disease
syndrome
disease · Nervous System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Carbohydrate Deficient Glycoprotein Syndrome Type 1O
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Carbohydrate Deficient Glycoprotein Syndrome Type 2K
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
Carbohydrate Intolerance
syndrome
disease · Digestive System Diseases; Nutritional and Metabolic Diseases
Carbohydrate Metabolism, Inborn Errors
group
group · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Carbon Monoxide Poisoning
disease
disease · Chemically-Induced Disorders
Carbonic Anhydrase I Deficiency
disease
disease
Carbonic Anhydrase I, Guam
phenotype
phenotype
Carbonic Anhydrase Ii Variant
phenotype
phenotype
Carbonic Anhydrase Va Deficiency, Hyperammonemia Due To
syndrome
disease
Carboxypeptidase N Deficiency
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Carbuncle/Furuncle
syndrome
disease · Skin and Connective Tissue Diseases; Infections
Carcinogenesis
phenotype
phenotype · Neoplasms; Pathological Conditions, Signs and Symptoms
Carcinogenesis, Radiation
phenotype
phenotype · Neoplasms; Pathological Conditions, Signs and Symptoms