LIST OF POSSIBLE DISEASES (Metabolic Diseases)
(Clic here to try diagnostic from symptoms)

- Acid-Base Imbalance -- Brain Diseases, Metabolic -- Calcium Metabolism Disorders -- DNA Repair-Deficiency Disorders -- Glucose Metabolism Disorders -- Iron Metabolism Disorders -- Lipid Metabolism Disorders -- Malabsorption Syndromes -- Metabolism, Inborn Errors -- Mitochondrial Diseases -- Phosphorus Metabolism Disorders -- Porphyrias -- Proteostasis Deficiencies -- Skin Diseases, Metabolic -- Wasting Syndrome -- Water-Electrolyte Imbalance -

A

Abetalipoproteinemia
Acatalasia
Achlorhydria
Acid-Base Imbalance
Acidosis
Acidosis, Lactic
Acidosis, Renal Tubular
Acidosis, Respiratory
Adiposis Dolorosa
Adrenal Hyperplasia, Congenital
Adrenoleukodystrophy
Albinism
Albinism, Ocular
Albinism, Oculocutaneous
Alexander Disease
Alkalosis
Alkalosis, Respiratory
Alkaptonuria

a

alpha-Mannosidosis

A

Amino Acid Metabolism, Inborn Errors
Amino Acid Transport Disorders, Inborn
Amyloid Neuropathies
Amyloid Neuropathies, Familial
Amyloidosis
Amyloidosis, Familial
Amyotrophic Lateral Sclerosis
Anemia, Iron-Deficiency
Antley-Bixler Syndrome Phenotype
Argininosuccinic Aciduria
Arthritis, Gouty
Aspartylglucosaminuria
Ataxia Telangiectasia

B

Barth Syndrome

b

beta-Mannosidosis

B

Biotinidase Deficiency
Blind Loop Syndrome
Bloom Syndrome
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn

C

Calcinosis
Calciphylaxis
Calcium Metabolism Disorders
Canavan Disease
Carbamoyl-Phosphate Synthase I Deficiency Disease
Carbohydrate Metabolism, Inborn Errors
Celiac Disease
Cerebral Amyloid Angiopathy
Cerebral Amyloid Angiopathy, Familial
Cholesterol Ester Storage Disease
Chondrodysplasia Punctata, Rhizomelic
Citrullinemia
Cockayne Syndrome
Collagenous Sprue
Colorectal Neoplasms, Hereditary Nonpolyposis
Congenital Disorders of Glycosylation
Congenital Hyperinsulinism
Coproporphyria, Hereditary
CREST Syndrome
Crigler-Najjar Syndrome
Cystinosis
Cystinuria
Cytochrome-c Oxidase Deficiency

D

Decalcification, Pathologic
Dehydration
Dent Disease
Diabetes Mellitus
Diabetes Mellitus, Experimental
Diabetes Mellitus, Lipoatrophic
Diabetes Mellitus, Type 1
Diabetes Mellitus, Type 2
Diabetes, Gestational
Diabetic Ketoacidosis
Dihydropyrimidine Dehydrogenase Deficiency
DNA Repair-Deficiency Disorders
Donohue Syndrome
Dyslipidemias

F

Fabry Disease
Familial Hypophosphatemic Rickets
Fanconi Anemia
Fanconi Syndrome
Farber Lipogranulomatosis
Friedreich Ataxia
Frontotemporal Dementia
Frontotemporal Lobar Degeneration
Fructose Intolerance
Fructose Metabolism, Inborn Errors
Fructose-1,6-Diphosphatase Deficiency
Fucosidosis

G

Galactosemias
Gangliosidoses
Gangliosidoses, GM2
Gangliosidosis, GM1
Gaucher Disease
Gilbert Disease
Gitelman Syndrome
Glucose Intolerance
Glucose Metabolism Disorders
Glucosephosphate Dehydrogenase Deficiency
Glycogen Storage Disease
Glycogen Storage Disease Type I
Glycogen Storage Disease Type II
Glycogen Storage Disease Type IIb
Glycogen Storage Disease Type III
Glycogen Storage Disease Type IV
Glycogen Storage Disease Type V
Glycogen Storage Disease Type VI
Glycogen Storage Disease Type VII
Glycogen Storage Disease Type VIII
Glycosuria
Glycosuria, Renal
Gout

H

Hartnup Disease
Hemochromatosis
Hemosiderosis
Hepatic Encephalopathy
Hepatolenticular Degeneration
Hereditary Central Nervous System Demyelinating Diseases
Hermanski-Pudlak Syndrome
HIV Wasting Syndrome
HIV-Associated Lipodystrophy Syndrome
Holocarboxylase Synthetase Deficiency
Homocystinuria
Hyperargininemia
Hyperbilirubinemia, Hereditary
Hypercalcemia
Hypercholesterolemia
Hyperglycemia
Hyperglycinemia, Nonketotic
Hyperhomocysteinemia
Hyperinsulinism
Hyperkalemia
Hyperlipidemia, Familial Combined
Hyperlipidemias
Hyperlipoproteinemia Type I
Hyperlipoproteinemia Type II
Hyperlipoproteinemia Type III
Hyperlipoproteinemia Type IV
Hyperlipoproteinemia Type V
Hyperlipoproteinemias
Hyperlysinemias
Hypernatremia
Hyperoxaluria, Primary
Hyperphosphatemia
Hypertriglyceridemia
Hypertriglyceridemic Waist
Hypoalphalipoproteinemias
Hypobetalipoproteinemia, Familial, Apolipoprotein B
Hypobetalipoproteinemias
Hypocalcemia
Hypoglycemia
Hypokalemia
Hypokalemic Periodic Paralysis
Hypolipoproteinemias
Hyponatremia
Hypophosphatasia
Hypophosphatemia
Hypophosphatemia, Familial

I

Ichthyosis, X-Linked
Inappropriate ADH Syndrome
Insulin Coma
Insulin Resistance
Iron Metabolism Disorders
Iron Overload

J

Jaundice, Chronic Idiopathic

K

Kearns-Sayre Syndrome
Kernicterus
Ketosis

L

Lactose Intolerance
Lecithin Acyltransferase Deficiency
Leigh Disease
Lesch-Nyhan Syndrome
Leukodystrophy, Globoid Cell
Leukodystrophy, Metachromatic
Li-Fraumeni Syndrome
Liddle Syndrome
Lipid Metabolism Disorders
Lipid Metabolism, Inborn Errors
Lipidoses
Lipodystrophy
Lipodystrophy, Congenital Generalized
Lipodystrophy, Familial Partial
Lipomatosis
Lipomatosis, Multiple Symmetrical
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System

M

Malabsorption Syndromes
Mannosidase Deficiency Diseases
Maple Syrup Urine Disease
MELAS Syndrome
Menkes Kinky Hair Syndrome
MERRF Syndrome
Metabolic Syndrome X
Metabolism, Inborn Errors
Metal Metabolism, Inborn Errors
Mevalonate Kinase Deficiency
Mineralocorticoid Excess Syndrome, Apparent
Mitochondrial Diseases
Mitochondrial Encephalomyopathies
Mitochondrial Myopathies
Monckeberg Medial Calcific Sclerosis
Mucolipidoses
Mucopolysaccharidoses
Mucopolysaccharidosis I
Mucopolysaccharidosis II
Mucopolysaccharidosis III
Mucopolysaccharidosis IV
Mucopolysaccharidosis VI
Mucopolysaccharidosis VII
Multiple Acyl Coenzyme A Dehydrogenase Deficiency
Multiple Carboxylase Deficiency
Multiple Sulfatase Deficiency Disease
Myelinolysis, Central Pontine

N

Necrobiosis Lipoidica
Necrobiotic Xanthogranuloma
Nephrocalcinosis
Nesidioblastosis
Neuronal Ceroid-Lipofuscinoses
Niemann-Pick Disease, Type A
Niemann-Pick Disease, Type B
Niemann-Pick Disease, Type C
Niemann-Pick Diseases
Nijmegen Breakage Syndrome

O

Oculocerebrorenal Syndrome
Ophthalmoplegia, Chronic Progressive External
Optic Atrophy, Autosomal Dominant
Optic Atrophy, Hereditary, Leber
Ornithine Carbamoyltransferase Deficiency Disease
Osteomalacia

P

Paralyses, Familial Periodic
Paralysis, Hyperkalemic Periodic
Pelizaeus-Merzbacher Disease
Peroxisomal Disorders
Phenylketonuria, Maternal
Phenylketonurias
Phosphorus Metabolism Disorders
Piebaldism
Porphyria Cutanea Tarda
Porphyria, Acute Intermittent
Porphyria, Erythropoietic
Porphyria, Hepatoerythropoietic
Porphyria, Variegate
Porphyrias
Porphyrias, Hepatic
Prediabetic State
Primary Progressive Nonfluent Aphasia
Progeria
Propionic Acidemia
Proteostasis Deficiencies
Protoporphyria, Erythropoietic
Pseudohypoaldosteronism
Pseudohypoparathyroidism
Pseudopseudohypoparathyroidism
Purine-Pyrimidine Metabolism, Inborn Errors
Pycnodysostosis
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Pyruvate Metabolism, Inborn Errors

R

Refsum Disease
Refsum Disease, Infantile
Renal Aminoacidurias
Renal Osteodystrophy
Renal Tubular Transport, Inborn Errors
Reye Syndrome
Rickets
Rickets, Hypophosphatemic
Rothmund-Thomson Syndrome

S

Sandhoff Disease
Sea-Blue Histiocyte Syndrome
Severe Combined Immunodeficiency
Sialic Acid Storage Disease
Sjogren-Larsson Syndrome
Skin Diseases, Metabolic
Smith-Lemli-Opitz Syndrome
Sphingolipidoses
Sprue, Tropical
Steatorrhea
Steroid Metabolism, Inborn Errors
Sulfatidosis

T

Tangier Disease
Tay-Sachs Disease
Tay-Sachs Disease, AB Variant
TDP-43 Proteinopathies
Tetany
Tyrosinemias

U

Urea Cycle Disorders, Inborn

V

Vascular Calcification

W

Wasting Syndrome
Water Intoxication
Water-Electrolyte Imbalance
Werner Syndrome
Wernicke Encephalopathy
Whipple Disease
Wolfram Syndrome
Wolman Disease

X

Xanthomatosis
Xanthomatosis, Cerebrotendinous
Xeroderma Pigmentosum

Z

Zellweger Syndrome

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