Skip to main content

Table 2 Top tier ranked up to 10th associated diseases

From: CLASH: Complementary Linkage with Anchoring and Scoring for Heterogeneous biomolecular and clinical data

Target Disease

Associated via Reference Network

Associated via Complemented Network

Celiac Disease

Diabetes Mellitus

Metabolic Syndrome X

Glucose Intolerance

Hyperinsulinism

Hyperlipidemias

Calcinosis

Dyslipidemias

Hyperhomocysteinemia

Anemia, Iron-Deficiency

Homochromatosis

Diabetes Mellitus

Metabolic Syndrome X

Glucose Intolerance

Hyperinsulinism

Congentital Hyperinsulinism**

Malabsorption Syndromes*

Hypoglycemia**

Dyslipidemais

Hyperglycemia**

Hyperhomocysteinemia†

Lactose Intolerance

Diabetes Mellitus

Metabolic Syndrome X

Glucose Intolerance

Celiac Disease

Dyslipidemias

Hyperinsulinism

Amyotrophic Lateral Sclerosis

Insulin Resistance

Hyperlipidemias

Glucose Metabolism Disorders

Mucolipidoses*

Celiac Disease*

Glycogen Storage Disease*

Metabolism, Inborn Errors*

Malabsorption Syndromes*

Diabetes Mellitus

Hypoglycemia**

Hyperinsulinism**

Glucose Intolerance**

Hypokalemia*

Hypophosphatasia

Metabolic Syndrome X

Diabetes Mellitus

Glucose Intolerance

Metabolic Diseases

Dyslipidemias

Amyotrophic Lateral Sclerosis

Diabetes, Gestational

Hyperlipidemias

Hyperinsulinism

Calcinosis

Acidosis, Renal Tubular*

Zellweger Syndrome*

Celiac Disease*

Peroxisomal Disorders**

Refsum Disease*

Metabolism, Inborn Errors*

Adrenoleukodystrophy*

Homocystinuria**

Diabetes Mellitus

Phenylketonurias*

Refsum Disease

Zellweger Syndrome

Peroxisomal Disorders

Chondrodysplasia Punctata, Rhizomelic

Adrenoleukodystrophy

Homocystinuria

Porphyrias

Protoporphyria, Erythropoietic

Hyperhomocysteinemia

Diabetic Ketoacidosis

Lipid Metabolism, Inborn Errors

Neuronal Ceroid-Lipofuscinoses*

Lipidoses*

Peroxisomal Disorders

Zellweger Syndrome

Diabetes Mellitus*

Leigh Disease*

Glycogen Storage Disease*

Adrenoleukodystrophy

Malabsorption Syndromes*

Glucose Intolerance**

Fanconi

Syndrome

Hypophosphatemia

Glycogen Storage Disease

Hypercalcemia

Glucose Intolerance

Metal Metabolism, Inborn Errors

Osteomalacia

Xanthomatosis, Cerebrotendinous

Diabetes Mellitus

Calcinosis

Metabolic Syndrome X

Celiac Disease*

Glycogen Storage Disease

Diabetes Mellitus

Carbohydrate Metabolism, Inborn Errors*

Leigh Disease*

Diabetes, Gestational*

Glucose Intolerance

Hyperinsulinism*

Hypoglycemia*

Congenital Hyperinsulinism**

Menkes Kinky Hair Syndrome

N/A

Congenital Disorders of Glycosylation*

Hyperglycinemia, Nonketotic*

Zellweger Syndrome*

Peroxisomal Disorders**

Hepatolenticular Degeneration*

Refsum Disease**

Acidosis, Lactic*

Albinism*

Mitochondrial Myopathies*

Adrenoleukodystrophy**

Pyruvate Carboxylase Deficiency

Disease

N/A

Acidosis, Renal Tubular*

Carbohydrate Metabolism, Inborn Errors*

Hyperglycinemia, Nonketotic*

Maple Syrup Urine Disease*

Glycogen Storage Disease*

Amino Acid Metabolism, Inborn Errors*

Renal Aminoacidurias**

Metabolism, Inborn Errors*

Acidosis, Lactic*

Pyruvate Metabolism, Inborn Errors*

Rothmund-Thomson Syndrome

N/A

DNA Repair-Deficiency Disorders*

Celiac Disease*

Metal Metabolism, Inborn Errors**

Acidosis*

Xanthomatosis, Cerebrotendinous**

Hypercalcemia*

Skin Diseases, Metabolic*

Amyloidosis, Familial*

Achlorhydria**

Osteomalacia**

Sphingolipidoses

N/A

Neuronal Ceroid-Lipofuscinoses*

Lipidoses*

Carbohydrate Metabolism, Inborn Errors*

Diabetes Mellitus*

Peroxisomal Disorders*

Zellweger Syndrome**

Glycogen Storage Disease*

Adrenoleukodystrophy*

Refsum Disease*

Glucose Intolerance**

Alkaptonuria

N/A

Carbohydrate Metabolism, Inborn Errors*

Glycogen Storage Disease*

Zellweger Syndrome*

Metabolism, Inborn Errors*

Peroxisomal Disorders**

Amino Acid Metabolism, Inborn Errors*

Refsum Disease*

Adrenoleukodystrophy**

Diabetes Mellitus*

Lipid Metabolism, Inborn Errors*

  1. Notations ‘’, ‘*’ and ‘**’ are identical to those in Fig. 5