Condition
30,467 condition in the knowledge graph · page 22.
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Acanthoma, Clear Cell
disease
disease · Neoplasms
Acanthomatous Ameloblastoma
disease
disease · Neoplasms
Acanthosis
phenotype
phenotype · Pathological Conditions, Signs and Symptoms
Acanthosis Nigricans
syndrome
ICD-10 L83
disease · Skin and Connective Tissue Diseases
Acanthosis Palmaris
syndrome
disease
Acatalasemia Japanese Type
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Acatalasemia Swiss Type
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Acatalasia
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Accelerated Atherosclerosis
phenotype
phenotype · Cardiovascular Diseases
Accelerated Bone Age After Puberty
phenotype
phenotype
Accelerated Idioventricular Rhythm
syndrome
disease · Cardiovascular Diseases; Pathological Conditions, Signs and Symptoms
Accelerated Tumor Formation, Susceptibility To
phenotype
phenotype
Accessory Carpal Bones
disease
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Accessory Hepatic Duct
disease
disease · Digestive System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Accessory Kidney
disease
ICD-10 Q63.0
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Accessory Nipple
disease
ICD-10 Q83.3
disease · Skin and Connective Tissue Diseases
Accessory Oral Frenulum
disease
disease
Accessory Rib
disease
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Accessory Scrotum
disease
disease
Accessory Skeletal Muscle
disease
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Accessory Spleen
disease
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Accidental Falls
phenotype
phenotype
Accommodation Phosphene Disorder
syndrome
disease
Accumulation of Melanosomes In Melanocytes
phenotype
phenotype
Accumulation of Muscle Fiber Desmin
phenotype
phenotype
Acephalic Spermatozoa
syndrome
disease
Acetabular Spurs
phenotype
phenotype
Acetyl-Coa: Carboxylase Deficiency
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Achalasia
syndrome
disease
Ache
phenotype
phenotype · Pathological Conditions, Signs and Symptoms
Acheiropodia
disease
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Achilles Tendinitis
syndrome
ICD-10 M76.6
disease · Wounds and Injuries; Musculoskeletal Diseases
Achlorhydria
phenotype
phenotype · Digestive System Diseases; Nutritional and Metabolic Diseases
Acholic Stool
phenotype
phenotype · Digestive System Diseases
Achondrogenesis
disease
ICD-10 Q77.0
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Achondrogenesis Type 1A
disease
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Achondrogenesis Type 2
disease
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Achondrogenesis, Type Ib (Disorder)
disease
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Achondroplasia
disease
ICD-10 Q77.4
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans
disease
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Achondroplastic Dwarfism
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Achromatic Retinal Patches
phenotype
phenotype
Achromatopsia
syndrome
disease · Eye Diseases; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Achromatopsia 1
syndrome
disease · Eye Diseases; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Achromatopsia 2
syndrome
disease · Eye Diseases; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Achromatopsia 3
syndrome
disease · Eye Diseases; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Achromatopsia 4
syndrome
disease · Eye Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Achromatopsia 5
syndrome
disease · Eye Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and Symptoms