Condition
30,467 condition in the knowledge graph · page 49.
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Amelogenesis Imperfecta, Type Ih
syndrome
disease
Amelogenesis Imperfecta, Type Iii
syndrome
disease · Stomatognathic Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Amelogenesis Imperfecta, Type Iiib
syndrome
disease
Amelogenesis Imperfecta, Type Ij
disease
disease
Amelogenesis Imperfecta, Type Iv
syndrome
disease · Stomatognathic Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Amenorrhea
phenotype
ICD-10 N91.2
phenotype · Pathological Conditions, Signs and Symptoms
American Cutaneous Leishmaniasis
syndrome
disease · Skin and Connective Tissue Diseases; Infections
Ametropia
syndrome
disease · Eye Diseases
Amino Acid Metabolism, Inborn Errors
group
ICD-10 E72.9
group · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Amino Acid Metabolism, Inherited Disorders
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Amino Acid Transport Disorder
group
ICD-10 E72.0
group · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Amino Acidemias
group
group
Amino Acids Measurement
group
group
Aminoacidemia
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Aminoaciduria
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Aminoacylase 1 Deficiency
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Aminoacylase 2 Deficiency
syndrome
disease · Nervous System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Aminopterin Syndrome Sine Aminopterin
syndrome
disease · Mental Disorders; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Behavior and Behavior Mechanisms; Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
Amish Brittle Hair Brain Syndrome
syndrome
disease · Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Amish Infantile Epilepsy Syndrome
syndrome
disease · Nervous System Diseases
Aml M5B
disease
disease
Amnesia
disease
disease · Behavior and Behavior Mechanisms; Mental Disorders; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Amnesia, Transient Global
disease
ICD-10 G45.4
disease · Behavior and Behavior Mechanisms; Mental Disorders; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Amnestic Disorder
disease
disease · Mental Disorders
Amnestic State
phenotype
phenotype · Behavior and Behavior Mechanisms; Mental Disorders; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Amniotic Bands
disease
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Amniotic Fluid Meconium Stained
phenotype
phenotype
Amotivation
phenotype
phenotype
Amphetamine Abuse
disease
disease · Mental Disorders; Chemically-Induced Disorders
Amphetamine Addiction
disease
disease · Mental Disorders; Chemically-Induced Disorders
Amphetamine Or Related Acting Sympathomimetic Abuse
disease
disease · Mental Disorders; Chemically-Induced Disorders
Amphetamine Withdrawal
disease
disease · Mental Disorders; Chemically-Induced Disorders
Amphetamine-Related Disorders
group
group · Mental Disorders; Chemically-Induced Disorders
Amputated Structure (Morphologic Abnormality)
phenotype
phenotype · Wounds and Injuries
Amputation Stumps
disease
disease
Amr Syndrome
syndrome
disease · Mental Disorders; Nervous System Diseases; Behavior and Behavior Mechanisms; Skin and Connective Tissue Diseases; Pathological Conditions, Signs and Symptoms
Amygdalo-Hippocampal Epilepsy
syndrome
disease · Nervous System Diseases
Amylo-1,6-Glucosidase Deficiency
syndrome
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Amyloid Angiopathy
syndrome
disease · Cardiovascular Diseases; Nervous System Diseases; Nutritional and Metabolic Diseases
Amyloid Cardiomyopathy, Transthyretin-Related
syndrome
disease
Amyloid Deposition In The Vitreous Humor
phenotype
phenotype
Amyloid Nephropathy
syndrome
disease · Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Nutritional and Metabolic Diseases; Pathological Conditions, Signs and Symptoms
Amyloid Neuropathies
syndrome
disease · Nervous System Diseases; Nutritional and Metabolic Diseases
Amyloid Neuropathies, Familial
group
ICD-10 E85.1
group · Nervous System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Amyloid of Cornea
syndrome
disease
Amyloid of Vitreous
syndrome
disease
Amyloid Polyneuropathy, British Type (Disorder)
syndrome
disease · Nervous System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Amyloid Polyneuropathy, Iowa Type
syndrome
disease · Nervous System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases