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About:
http://dbpedia.org/class/yago/WikicatMetabolicDisorders
An Entity of Type:
Thing
,
from Named Graph:
http://dbpedia.org
,
within Data Space:
dbpedia.org
Property
Value
rdfs:
subClassOf
yago
:MetabolicDisorder114084502
owl:
equivalentClass
yago-res
:wikicat_Metabolic_disorders
is
rdf:
type
of
dbr
:Sanfilippo_syndrome
dbr
:Schindler_disease
dbr
:Mitochondrial_disease
dbr
:MEFV
dbr
:Metab-L
dbr
:Metabolic_myopathy
dbr
:Metabolic_syndrome
dbr
:Metachromatic_leukodystrophy
dbr
:Metastatic_calcification
dbr
:Primary_polydipsia
dbr
:Barth_syndrome
dbr
:Biotinidase_deficiency
dbr
:Anion_gap
dbr
:Arakawa's_syndrome_II
dbr
:Homocystinuria
dbr
:Hurler–Scheie_syndrome
dbr
:Hyaluronidase_deficiency
dbr
:Hyperammonemia
dbr
:Hypertriglyceridemia
dbr
:Hypophosphatasia
dbr
:Beta-mannosidosis
dbr
:Cushing's_syndrome
dbr
:Cystinuria
dbr
:Dopamine_beta_hydroxylase_deficiency
dbr
:Dyslipidemia
dbr
:Dystrophic_calcification
dbr
:Infantile_neuronal_ceroid_lipofuscinosis
dbr
:Insulin_resistance
dbr
:Iodine_deficiency
dbr
:Jamaican_vomiting_sickness
dbr
:Leucism
dbr
:Leukodystrophy
dbr
:Steatosis
dbr
:Rosenthal_fiber
dbr
:Urea_cycle_disorder
dbr
:Crigler–Najjar_syndrome
dbr
:Amyloid_beta
dbr
:Maturity_onset_diabetes_of_the_young
dbr
:Menkes_disease
dbr
:Salicylate_sensitivity
dbr
:Erythropoietic_protoporphyria
dbr
:Citrullinemia
dbr
:Epidermodysplasia_verruciformis
dbr
:Gaucher's_disease
dbr
:Gilbert's_syndrome
dbr
:Glycogen_storage_disease_type_I
dbr
:Glycogen_storage_disease_type_II
dbr
:Glycogen_storage_disease_type_III
dbr
:Glycogen_storage_disease_type_IV
dbr
:Glycogen_storage_disease_type_VI
dbr
:Glycogen_storage_disease_type_XI
dbr
:Morquio_syndrome
dbr
:Lactic_acidosis
dbr
:Lafora_disease
dbr
:Maroteaux–Lamy_syndrome
dbr
:Milk-alkali_syndrome
dbr
:Alpha_1-antitrypsin_deficiency
dbr
:Organic_acidemia
dbr
:Androgen_insensitivity_syndrome
dbr
:Batten_disease
dbr
:Lecithin_cholesterol_acyltransferase_deficiency
dbr
:Lesch–Nyhan_syndrome
dbr
:Lipodystrophy
dbr
:Lipoprotein_lipase_deficiency
dbr
:Calcinosis
dbr
:Chondrocalcinosis
dbr
:Sitosterolemia
dbr
:Sleeve_gastrectomy
dbr
:Smith–Lemli–Opitz_syndrome
dbr
:Fructose_malabsorption
dbr
:Fumarase_deficiency
dbr
:Diabetes_mellitus_type_1
dbr
:Diabetes_mellitus_type_2
dbr
:Porphyria_cutanea_tarda
dbr
:Pulmonary_alveolar_proteinosis
dbr
:Trimethylaminuria
dbr
:6-Pyruvoyltetrahydropterin_synthase_deficiency
dbr
:Acute_intermittent_porphyria
dbr
:Adenosine_deaminase_deficiency
dbr
:Adenosine_monophosphate_deaminase_deficiency_type_1
dbr
:Adiposis_dolorosa
dbr
:Trichothiodystrophy
dbr
:Tyrosinemia_type_II
dbr
:Wilson's_disease
dbr
:Dubin–Johnson_syndrome
dbr
:Galactosialidosis
dbr
:Gangliosidosis
dbr
:HIV-associated_lipodystrophy
dbr
:Hartnup_disease
dbr
:Lipoatrophy
dbr
:Long-chain_3-hydroxyacyl-coenzyme_A_dehydrogenase_deficiency
dbr
:Pentosuria
dbr
:Winchester_syndrome
dbr
:3-Methylglutaconic_aciduria
dbr
:Acatalasia
dbr
:Adjustable_gastric_band
dbr
:Adrenoleukodystrophy
dbr
:Alström_syndrome
dbr
:Amyloid_precursor_protein
dbr
:Cystinosis
dbr
:Alpha-mannosidosis
dbr
:Alzheimer's_disease
dbr
:Fabry_disease
dbr
:Familial_Mediterranean_fever
dbr
:Bariatric_surgery
dbr
:Niemann–Pick_disease
dbr
:Niemann–Pick_disease,_type_C
dbr
:Chylomicron_retention_disease
dbr
:Danon_disease
dbr
:Diabetic_ketoacidosis
dbr
:Fanconi_syndrome
dbr
:Farber_disease
dbr
:Food_intolerance
dbr
:Glutaric_aciduria_type_1
dbr
:Glycogen_storage_disease
dbr
:Glycogen_storage_disease_type_V
dbr
:Histidinemia
dbr
:Kayser–Fleischer_ring
dbr
:Lucey–Driscoll_syndrome
dbr
:Refsum_disease
dbr
:Hepatic_encephalopathy
dbr
:Hereditary_fructose_intolerance
dbr
:Hereditary_hyperbilirubinemia
dbr
:Asterixis
dbr
:Atransferrinemia
dbr
:Jansky–Bielschowsky_disease
dbr
:Tangier_disease
dbr
:Tay–Sachs_disease
dbr
:Hunter_syndrome
dbr
:Hurler_syndrome
dbr
:Hyperhomocysteinemia
dbr
:Hyperosmolar_hyperglycemic_state
dbr
:Hyperoxaluria
dbr
:Hyperuricemia
dbr
:Hypervitaminosis_A
dbr
:Hypophosphatemia
dbr
:Tetanic_contraction
dbr
:Argininemia
dbr
:Aceruloplasminemia
dbr
:Acrodermatitis_enteropathica
dbr
:Advanced_glycation_end-product
dbr
:Alcohol_flush_reaction
dbr
:Blue_diaper_syndrome
dbr
:Hereditary_coproporphyria
dbr
:Heredofamilial_amyloidosis
dbr
:Holocarboxylase_synthetase_deficiency
dbr
:Wolman_disease
dbr
:Zellweger_syndrome
dbr
:Krabbe_disease
dbr
:Refeeding_syndrome
dbr
:Cerebrotendineous_xanthomatosis
dbr
:X-linked_hypophosphatemia
dbr
:Xanthinuria
dbr
:MDP_syndrome
dbr
:Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency
dbr
:Mevalonate_kinase_deficiency
dbr
:Multiple_sulfatase_deficiency
dbr
:Rotor_syndrome
dbr
:Sjögren–Larsson_syndrome
dbr
:Waardenburg_syndrome
dbr
:Gunther_disease
dbr
:Lysosomal_storage_disease
dbr
:Lysosomal_acid_lipase_deficiency
dbr
:Steatohepatitis
dbr
:Sea-blue_histiocytosis
dbr
:Triosephosphate_isomerase_deficiency
dbr
:Exercise-associated_hyponatremia
dbr
:Gestational_diabetes
dbr
:Scheie_syndrome
dbr
:Wernicke's_encephalopathy
dbr
:Molybdenum_cofactor_deficiency
dbr
:Salla_disease
dbr
:Mucolipidosis
dbr
:Inborn_errors_of_metal_metabolism
dbr
:Phosphofructokinase_deficiency
dbr
:Toxic_multinodular_goitre
dbr
:Sedentary_lifestyle
dbr
:Sucrose_intolerance
dbr
:Type_I_tyrosinemia
dbr
:X-linked_ichthyosis
dbr
:Pansteatitis
dbr
:Latent_autoimmune_diabetes_of_adults
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