Condition
144 condition in the knowledge graph · page 2.
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Gigantism And Acromegaly
syndrome
ICD-10 E22.0
disease · Nervous System Diseases; Endocrine System Diseases
Gilbert Disease (Disorder)
syndrome
ICD-10 E80.4
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Glycogen Storage Disease
group
ICD-10 E74.0
group · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Hyperaldosteronism
syndrome
ICD-10 E26; E26.9
disease · Endocrine System Diseases
Hyperestrogenism
syndrome
ICD-10 E28.0
disease
Hyperkalemia
phenotype
ICD-10 E87.5
phenotype · Nutritional and Metabolic Diseases
Hyperlipidemia
syndrome
ICD-10 E78.5
disease · Nutritional and Metabolic Diseases
Hyperlipidemia, Group A
syndrome
ICD-10 E78.0
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Hyperlipoproteinemia Type I
syndrome
ICD-10 E78.3
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Hyperlipoproteinemia Type Iv
syndrome
ICD-10 E78.1
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Hyperparathyroidism
syndrome
ICD-10 E21.3
disease · Endocrine System Diseases
Hyperparathyroidism, Primary
syndrome
ICD-10 E21.0
disease · Endocrine System Diseases
Hyperprolactinemia
syndrome
ICD-10 E22.1
disease · Nervous System Diseases; Endocrine System Diseases
Hyperuricemia Without Signs of Inflammatory Arthritis And Tophaceous Disease
syndrome
ICD-10 E79.0
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Pathological Conditions, Signs and Symptoms
Hypervitaminosis D
syndrome
ICD-10 E67.3
disease
Hypocupremia
syndrome
ICD-10 E61.0
disease
Hypoglycemia
syndrome
ICD-10 E16.2
disease · Nutritional and Metabolic Diseases
Hypokalemia
phenotype
ICD-10 E87.6
phenotype · Nutritional and Metabolic Diseases
Hypolipoproteinemias
phenotype
ICD-10 E78.6
phenotype · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Hypoparathyroidism
syndrome
ICD-10 E20.9; E20
disease · Endocrine System Diseases
Hypopituitarism
syndrome
ICD-10 E23.0
disease · Nervous System Diseases; Endocrine System Diseases
Hypothyroidism
syndrome
ICD-10 E03.9
disease · Endocrine System Diseases
Hypovolemia
phenotype
ICD-10 E86
phenotype · Pathological Conditions, Signs and Symptoms
Idiopathic Hypoparathyroidism
syndrome
ICD-10 E20.0
disease · Endocrine System Diseases
Imbalance of Constituents of Food Intake
phenotype
ICD-10 E63.1
phenotype · Nutritional and Metabolic Diseases
Inappropriate Adh Syndrome
phenotype
ICD-10 E22.2
phenotype · Nervous System Diseases; Nutritional and Metabolic Diseases; Endocrine System Diseases
Iron Deficiency
syndrome
ICD-10 E61.1
disease · Nutritional and Metabolic Diseases
Iron Metabolism Disorders
group
ICD-10 E83.1
group · Nutritional and Metabolic Diseases
Kwashiorkor
syndrome
ICD-10 E40
disease · Nutritional and Metabolic Diseases
Lactase Deficiency, Congenital
phenotype
ICD-10 E73.0
phenotype · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Lactose Intolerance
syndrome
ICD-10 E73; E73.9
disease · Digestive System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Lesch-Nyhan Syndrome
syndrome
ICD-10 E79.1
disease · Nervous System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Lipodystrophy, Not Elsewhere Classified
syndrome
ICD-10 E88.1
disease · Skin and Connective Tissue Diseases; Nutritional and Metabolic Diseases
Lipoidosis
syndrome
ICD-10 E75.6
disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Magnesium Deficiency
syndrome
ICD-10 E61.2
disease · Nutritional and Metabolic Diseases
Malignant Carcinoid Syndrome
syndrome
ICD-10 E34.0
disease · Neoplasms
Malnutrition
syndrome
ICD-10 E40-E46.9; E63.9
disease · Nutritional and Metabolic Diseases
Malnutrition Related Diabetes Mellitus
syndrome
ICD-10 E12
disease · Nutritional and Metabolic Diseases; Endocrine System Diseases
Manganese Deficiency
syndrome
ICD-10 E61.3
disease
Maple Syrup Urine Disease
syndrome
ICD-10 E71.0
disease · Nervous System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Marasmus
syndrome
ICD-10 E41
disease · Nutritional and Metabolic Diseases
Metabolic Diseases
group
ICD-10 E70-E90.9; E88.9
group · Nutritional and Metabolic Diseases
Mixed Hyperlipidemia (Disorder)
syndrome
ICD-10 E78.2
disease · Nutritional and Metabolic Diseases
Mucopolysaccharidoses
syndrome
ICD-10 E76.3
disease · Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Mucopolysaccharidosis I
syndrome
ICD-10 E76.0
disease · Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Mucopolysaccharidosis Ii
syndrome
ICD-10 E76.1
disease · Nervous System Diseases; Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Nelson Syndrome
disease
ICD-10 E24.1
disease · Nervous System Diseases; Neoplasms; Endocrine System Diseases
Neuronal Ceroid-Lipofuscinoses
syndrome
ICD-10 E75.4
disease · Nervous System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases