Condition
30,467 condition in the knowledge graph · page 60.
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Aortic Aneurysm, Familial Thoracic 9
syndrome
disease
Aortic Aneurysm, Ruptured
syndrome
ICD-10 I71.8
disease · Cardiovascular Diseases; Wounds and Injuries
Aortic Aneurysm, Thoracic
syndrome
disease · Cardiovascular Diseases
Aortic Aneurysm, Thoracoabdominal
syndrome
disease · Cardiovascular Diseases
Aortic Angiosarcoma
disease
disease
Aortic Arch Calcification
phenotype
phenotype
Aortic Coarctation
disease
ICD-10 Q25.1
disease · Cardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Aortic Diseases
group
group · Cardiovascular Diseases
Aortic Dissection Rupture
syndrome
disease
Aortic Intramural Haematoma
syndrome
disease
Aortic Root Dilatation
disease
disease · Cardiovascular Diseases
Aortic Root Dilation
syndrome
disease
Aortic Rupture
syndrome
disease · Cardiovascular Diseases; Wounds and Injuries
Aortic Sclerosis
syndrome
disease
Aortic Stenosis Symptomatic
syndrome
disease
Aortic Stiffness
phenotype
phenotype
Aortic Tortuosity
disease
disease
Aortic Valve Calcification
syndrome
disease · Cardiovascular Diseases; Nutritional and Metabolic Diseases
Aortic Valve Disease 1
syndrome
disease · Cardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Aortic Valve Disease 2
syndrome
disease
Aortic Valve Disorder
syndrome
ICD-10 I35.9
disease · Cardiovascular Diseases
Aortic Valve Insufficiency
syndrome
ICD-10 I35.1
disease · Cardiovascular Diseases
Aortic Valve Sclerosis
syndrome
disease · Cardiovascular Diseases; Nutritional and Metabolic Diseases
Aortic Valve Stenosis
syndrome
ICD-10 I35.0; Q25.3
disease · Cardiovascular Diseases
Aortic Wall Hypertrophy
syndrome
disease
Aortitis
syndrome
disease · Cardiovascular Diseases
Aortitis Syndrome
syndrome
disease · Cardiovascular Diseases; Skin and Connective Tissue Diseases
Aortocaval Fistula
disease
disease · Cardiovascular Diseases
Aortoiliac Occlusive Disease
syndrome
disease
Aortopulmonary Collateral Arteries
phenotype
phenotype
Aortopulmonary Septal Defect
disease
ICD-10 Q21.4
disease · Cardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Apathy
phenotype
phenotype · Behavior and Behavior Mechanisms
Apert Syndrome
disease
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Apert-Crouzon Disease
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Aphakia
disease
ICD-10 H27.0
disease · Eye Diseases
Aphakia, Congenital Primary
disease
disease · Eye Diseases
Aphalangy of The Hands
disease
disease
Aphasia
disease
disease · Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Aphasia, Acquired
disease
disease · Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Aphasia, Ageusic
phenotype
phenotype · Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Aphasia, Auditory Discriminatory
phenotype
phenotype · Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Aphasia, Commisural
phenotype
phenotype · Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Aphasia, Expressive
disease
disease · Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Aphasia, Functional
phenotype
phenotype · Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Aphasia, Global
disease
disease · Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Aphasia, Graphomotor
phenotype
phenotype · Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Aphasia, Intellectual
phenotype
phenotype · Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Aphasia, Mixed
disease
disease · Nervous System Diseases; Pathological Conditions, Signs and Symptoms