Condition
30,467 condition in the knowledge graph · page 23.
Popular condition searches — click any to filter
Achromatopsia 6
syndrome
disease
Achromatopsia 7
syndrome
disease
Achromatopsia Incomplete, X-Linked
syndrome
disease · Eye Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Achromia of Skin
phenotype
phenotype · Skin and Connective Tissue Diseases
Acid Cholesteryl Ester Hydrolase Deficiency, Type 2
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Acid Phosphatase Deficiency
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Acid Reflux
phenotype
phenotype
Acid-Labile Subunit Deficiency
disease
disease
Acidosis
phenotype
ICD-10 E87.2
phenotype · Nutritional and Metabolic Diseases
Acidosis, Lactic
phenotype
phenotype · Nutritional and Metabolic Diseases
Acidosis, Respiratory
phenotype
phenotype · Respiratory Tract Diseases; Nutritional and Metabolic Diseases
Aciduria
phenotype
phenotype
Acinar Cell Carcinoma
disease
disease · Neoplasms
Acinar Cell Carcinoma of Pancreas
disease
disease · Digestive System Diseases; Neoplasms; Endocrine System Diseases
Acinar Cell Cystadenoma
disease
disease
Acinar Cell Tumor
disease
disease · Neoplasms
Acinetobacter Bacteraemia
syndrome
disease
Acinetobacter Infections
group
group · Infections
Acinic Cell Carcinoma of Salivary Gland
disease
disease · Stomatognathic Diseases; Neoplasms
Acne
syndrome
ICD-10 L70.9; L70
disease · Skin and Connective Tissue Diseases
Acne Conglobata
syndrome
ICD-10 L70.1
disease · Skin and Connective Tissue Diseases
Acne Fulminans
syndrome
disease · Skin and Connective Tissue Diseases
Acne Inversa, Familial, 1
syndrome
disease · Skin and Connective Tissue Diseases; Infections
Acne Inversa, Familial, 2, With Or Without Dowling-Degos Disease
syndrome
disease
Acne Inversa, Familial, 3
syndrome
disease
Acne Keloid
syndrome
ICD-10 L73.0
disease · Skin and Connective Tissue Diseases
Acne Vulgaris
syndrome
ICD-10 L70.0
disease · Skin and Connective Tissue Diseases
Acoustic Neuroma
disease
disease · Nervous System Diseases; Otorhinolaryngologic Diseases; Neoplasms
Acquired Amegakaryocytic Thrombocytopenia
phenotype
phenotype · Immune System Diseases; Hemic and Lymphatic Diseases; Pathological Conditions, Signs and Symptoms
Acquired Angioedema
syndrome
disease · Cardiovascular Diseases; Skin and Connective Tissue Diseases; Immune System Diseases
Acquired Anomaly of Tongue
disease
disease · Stomatognathic Diseases
Acquired Antithrombin Iii Deficiency
syndrome
disease
Acquired Aplastic Anemia
syndrome
disease · Hemic and Lymphatic Diseases
Acquired Atrophy of Ovary
syndrome
disease · Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
Acquired C1 Inhibitor Deficiency
syndrome
disease · Cardiovascular Diseases; Skin and Connective Tissue Diseases; Immune System Diseases
Acquired Camptodactyly
disease
disease
Acquired Cjd
syndrome
disease · Mental Disorders; Animal Diseases; Infections; Nervous System Diseases
Acquired Clubfoot
disease
disease · Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases
Acquired Communicating Hydrocephalus
disease
disease · Nervous System Diseases
Acquired Cubitus Valgus
disease
disease
Acquired Cystic Disease Associated Renal Cell Carcinoma
disease
disease · Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Neoplasms
Acquired Cystic Kidney Disease
syndrome
disease
Acquired Deformity of Finger
disease
ICD-10 M20.0
disease · Musculoskeletal Diseases
Acquired Factor X Deficiency Disease
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Acquired Factor Xiii Deficiency
syndrome
disease
Acquired Fanconi Syndrome
syndrome
disease · Female Urogenital Diseases and Pregnancy Complications; Neoplasms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Male Urogenital Diseases; Immune System Diseases; Hemic and Lymphatic Diseases
Acquired Flat Foot
disease
ICD-10 M21.4
disease · Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Acquired Generalized Lipodystrophy
syndrome
disease · Skin and Connective Tissue Diseases; Nutritional and Metabolic Diseases; Endocrine System Diseases