Browse Medical Conditions by Category: Nutritional and Metabolic Diseases
- Mucolipidoses
- Mucopolysaccharidoses
- Mucopolysaccharidosis I
- Mucopolysaccharidosis II
- Mucopolysaccharidosis III
- Mucopolysaccharidosis IV
- Mucopolysaccharidosis VI
- Mucopolysaccharidosis VII
- Multiple Acyl Coenzyme A Dehydrogenase Deficiency
- Multiple Sulfatase Deficiency Disease
- Necrobiosis Lipoidica
- Nephrocalcinosis
- Nesidioblastosis
- Neuronal Ceroid-Lipofuscinoses
- Niemann-Pick Diseases
- Niemann-Pick Disease, Type A
- Niemann-Pick Disease, Type B
- Niemann-Pick Disease, Type C
- Nijmegen Breakage Syndrome
- Nutrition Disorders
- Obesity
- Obesity, Abdominal
- Obesity Hypoventilation Syndrome
- Obesity, Maternal
- Obesity, Metabolically Benign
- Obesity, Morbid
- Oculocerebrorenal Syndrome
- Ophthalmoplegia, Chronic Progressive External
- Optic Atrophy, Autosomal Dominant
- Optic Atrophy, Hereditary, Leber
- Ornithine Carbamoyltransferase Deficiency Disease
- Osteomalacia
- Osteoporosis
- Osteoporosis, Postmenopausal
- Overnutrition
- Paralysis, Hyperkalemic Periodic
- Pediatric Obesity
- Pelizaeus-Merzbacher Disease
- Peroxisomal Disorders
- Phenylketonuria, Maternal
- Phenylketonurias
- Phosphorus Metabolism Disorders
- Piebaldism
- Porphyria, Acute Intermittent
- Porphyria Cutanea Tarda
- Porphyria, Erythropoietic
- Porphyrias
- Porphyrias, Hepatic
- Porphyria, Variegate
- Potassium Deficiency
- Prader-Willi Syndrome
- Prediabetic State
- Primary Progressive Nonfluent Aphasia
- Progeria
- Propionic Acidemia
- Protein Deficiency
- Protein-Energy Malnutrition
- Proteostasis Deficiencies
- Protoporphyria, Erythropoietic
- Pseudohypoparathyroidism
- Pseudopseudohypoparathyroidism
- Purine-Pyrimidine Metabolism, Inborn Errors
- Pyruvate Carboxylase Deficiency Disease
- Pyruvate Dehydrogenase Complex Deficiency Disease
- Pyruvate Metabolism, Inborn Errors
- Refeeding Syndrome
- Refsum Disease
- Refsum Disease, Infantile
- Renal Tubular Transport, Inborn Errors
- Rickets
- Rickets, Hypophosphatemic
- Rothmund-Thomson Syndrome
- Sandhoff Disease
- Scurvy
- Severe Acute Malnutrition
- Severe Combined Immunodeficiency
- Shwachman-Diamond Syndrome
- Sialic Acid Storage Disease
- Sjogren-Larsson Syndrome
- Skin Diseases, Metabolic
- Smith-Lemli-Opitz Syndrome
- Sphingolipidoses
- Sprue, Tropical
- Starvation
- Steatitis
- Steatorrhea
- Steroid Metabolism, Inborn Errors
- Sulfatidosis
- Swayback
- Synucleinopathies
- Tangier Disease
- Tay-Sachs Disease
- Tay-Sachs Disease, AB Variant
- TDP-43 Proteinopathies
- Tetany
- Thiamine Deficiency
- Tyrosinemias
- Urea Cycle Disorders, Inborn
- Vascular Calcification
- Vitamin A Deficiency
- Vitamin B 6 Deficiency
- Vitamin B 12 Deficiency
- Vitamin D Deficiency
- Vitamin E Deficiency
- Vitamin K Deficiency
- Wasting Syndrome
- Water-Electrolyte Imbalance
- Water Intoxication
- Werner Syndrome
- Wernicke Encephalopathy
- Whipple Disease
- Wolfram Syndrome
- Wolman Disease
- Xanthomatosis
- Xanthomatosis, Cerebrotendinous
- Xeroderma Pigmentosum
- Zellweger Syndrome