Condition
144 condition in the knowledge graph.
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Acidosis
phenotype
ICD-10 E87.2
phenotype · Nutritional and Metabolic Diseases
Acth Syndrome, Ectopic
syndrome
ICD-10 E24.3
disease · Neoplasms
Addison Disease
syndrome
ICD-10 E27.1
disease · Immune System Diseases; Endocrine System Diseases
Addisonian Crisis
syndrome
ICD-10 E27.2
disease · Endocrine System Diseases; Pathological Conditions, Signs and Symptoms
Adrenal Gland Diseases
group
ICD-10 E27.9
group · Endocrine System Diseases
Adrenogenital Disorder
syndrome
ICD-10 E25.9; E25
disease · Endocrine System Diseases
Albinism
syndrome
ICD-10 E70.3
disease · Eye Diseases; Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Alkalosis
phenotype
ICD-10 E87.3
phenotype · Nutritional and Metabolic 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 Transport Disorder
group
ICD-10 E72.0
group · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; 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
Amyloidosis
syndrome
ICD-10 E85; E85.9
disease · Nutritional and Metabolic Diseases
Androgen-Insensitivity Syndrome
syndrome
ICD-10 E34.5
disease · Male Urogenital Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
Ascorbic Acid Deficiency
syndrome
ICD-10 E54
disease · Nutritional and Metabolic Diseases
Autoimmune Thyroiditis
syndrome
ICD-10 E06.3
disease · Immune System Diseases; Endocrine System Diseases
Beriberi
syndrome
ICD-10 E51.1
disease · Nutritional and Metabolic Diseases
Calcium Metabolism Disorders
group
ICD-10 E83.5
group · Nutritional and Metabolic Diseases
Classical Phenylketonuria
syndrome
ICD-10 E70.0
disease · Nervous System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Complications of Diabetes Mellitus
group
ICD-10 E14.8
group · Endocrine System Diseases
Congenital Hypothyroidism Without Goiter
syndrome
ICD-10 E03.1
disease · Endocrine System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Conn Syndrome
syndrome
ICD-10 E26.0
disease · Endocrine System Diseases
Crigler Najjar Syndrome, Type 1
syndrome
ICD-10 E80.5
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Cushing Syndrome
syndrome
ICD-10 E24.9; E24
disease · Endocrine System Diseases
Cystic Fibrosis
syndrome
ICD-10 E84.9; E84
disease · Digestive System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases
Delayed Puberty
phenotype
ICD-10 E30.0
phenotype · Endocrine System Diseases
Diabetes Insipidus
syndrome
ICD-10 E23.2
disease · Male Urogenital Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
Diabetes Mellitus
group
ICD-10 E10-E14.9; E14
group · Nutritional and Metabolic Diseases; Endocrine System Diseases
Diabetes Mellitus, Insulin-Dependent
syndrome
ICD-10 E10
disease · Immune System Diseases; Nutritional and Metabolic Diseases; Endocrine System Diseases
Diabetes Mellitus, Non-Insulin-Dependent
syndrome
ICD-10 E11
disease · Nutritional and Metabolic Diseases; Endocrine System Diseases
Diabetic Peripheral Angiopathy
syndrome
ICD-10 E14.5
disease · Cardiovascular Diseases; Nutritional and Metabolic Diseases; Endocrine System Diseases
Dietary Selenium Deficiency
phenotype
ICD-10 E59
phenotype
Dietary Zinc Deficiency
phenotype
ICD-10 E60
phenotype
Diffuse Goiter
syndrome
ICD-10 E04.0
disease · Endocrine System Diseases
Disorder of Branched-Chain Amino Acid Metabolism
group
ICD-10 E71.2
group · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Disorder of Carbohydrate Metabolism
group
ICD-10 E74.9
group · Nutritional and Metabolic Diseases
Disorder of Copper Metabolism
group
ICD-10 E83.0
group · Pathological Conditions, Signs and Symptoms
Disorder of Endocrine Ovary
group
ICD-10 E28.9; E28
group · Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
Disorder of Fatty Acid Metabolism
group
ICD-10 E71.3
group · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Pathological Conditions, Signs and Symptoms
Disorder of Galactose Metabolism
syndrome
ICD-10 E74.2
disease
Disorder of Glycoprotein Metabolism
group
ICD-10 E77.9; E77
group · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Disorder of Magnesium Metabolism
group
ICD-10 E83.4
group · Pathological Conditions, Signs and Symptoms
Disorder of Sulfur-Bearing Amino Acid Metabolism
phenotype
ICD-10 E72.1
phenotype · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Pathological Conditions, Signs and Symptoms
Dyshormonogenic Goiter
syndrome
ICD-10 E07.1
disease · Endocrine System Diseases
Endemic Goiter
syndrome
ICD-10 E01.0; E01.2
disease · Endocrine System Diseases
Endocrine System Diseases
group
ICD-10 E34.9
group · Endocrine System Diseases
Familial Non-Neuropathic Amyloidosis
syndrome
ICD-10 E85.0
disease · Nutritional and Metabolic Diseases
Fluid Overload
disease
ICD-10 E87.7
disease · Cardiovascular Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Nutritional and Metabolic Diseases
Gangliosidoses, Gm2
syndrome
ICD-10 E75.0
disease · Nervous System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
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