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About:
http://dbpedia.org/class/yago/WikicatAutosomalRecessiveDisorders
An Entity of Type:
Thing
,
from Named Graph:
http://dbpedia.org
,
within Data Space:
dbpedia.org
Property
Value
rdfs:
subClassOf
yago
:Disorder114052403
owl:
equivalentClass
yago-res
:wikicat_Autosomal_recessive_disorders
is
rdf:
type
of
dbr
:Carnitine_palmitoyltransferase_II_deficiency
dbr
:Cartilage–hair_hypoplasia
dbr
:Aminolevulinic_acid_dehydratase_deficiency_porphyria
dbr
:Behr_syndrome
dbr
:Primary_ciliary_dyskinesia
dbr
:Propionic_acidemia
dbr
:Pseudoxanthoma_elasticum
dbr
:Pyruvate_carboxylase_deficiency
dbr
:Sandhoff_disease
dbr
:Sanfilippo_syndrome
dbr
:Neuronal_ceroid_lipofuscinosis
dbr
:Nijmegen_breakage_syndrome
dbr
:MORM_syndrome
dbr
:Meleda_disease
dbr
:Metachromatic_leukodystrophy
dbr
:Nephronophthisis
dbr
:Persistent_Müllerian_duct_syndrome
dbr
:Omenn_syndrome
dbr
:Wolcott–Rallison_syndrome
dbr
:Prolidase_deficiency
dbr
:Sarcosinemia
dbr
:Bare_lymphocyte_syndrome
dbr
:Biotinidase_deficiency
dbr
:Apparent_mineralocorticoid_excess_syndrome
dbr
:Homocystinuria
dbr
:Beta-ketothiolase_deficiency
dbr
:Beta-mannosidosis
dbr
:Renal-hepatic-pancreatic_dysplasia
dbr
:Cystathioninuria
dbr
:Cystinuria
dbr
:DOOR_syndrome
dbr
:Usher_syndrome
dbr
:De_Barsy_syndrome
dbr
:Donohue_syndrome
dbr
:EEM_syndrome
dbr
:Infantile_Refsum_disease
dbr
:Infantile_neuroaxonal_dystrophy
dbr
:Jalili_syndrome
dbr
:Johanson–Blizzard_syndrome
dbr
:Lethal_congenital_contracture_syndrome
dbr
:Letterer–Siwe_disease
dbr
:Leukocyte_adhesion_deficiency
dbr
:Leukocyte_adhesion_deficiency-1
dbr
:Leydig_cell_hypoplasia
dbr
:Pendred_syndrome
dbr
:Pseudodominance
dbr
:Roberts_syndrome
dbr
:Meckel_syndrome
dbr
:Essential_fructosuria
dbr
:Genetic_studies_on_Arabs
dbr
:Woodhouse–Sakati_syndrome
dbr
:Vici_syndrome
dbr
:Oculocutaneous_albinism_type_I
dbr
:17-beta-hydroxysteroid_dehydrogenase_deficiency
dbr
:Citrullinemia
dbr
:Cockayne_syndrome
dbr
:Ellis–van_Creveld_syndrome
dbr
:Endocardial_fibroelastosis
dbr
:GM1_gangliosidoses
dbr
:GM2_gangliosidoses
dbr
:Galactose_epimerase_deficiency
dbr
:Gastroschisis
dbr
:Gaucher's_disease
dbr
:Gillespie_syndrome
dbr
:Glanzmann's_thrombasthenia
dbr
:Glycogen_storage_disease_type_I
dbr
:Glycogen_storage_disease_type_II
dbr
:Glycogen_storage_disease_type_III
dbr
:Mitochondrial_DNA_depletion_syndrome
dbr
:Morquio_syndrome
dbr
:Congenital_adrenal_hyperplasia
dbr
:Congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency
dbr
:Congenital_disorder_of_glycosylation_type_IIc
dbr
:Congenital_hepatic_fibrosis
dbr
:Congenital_ichthyosiform_erythroderma
dbr
:Congenital_insensitivity_to_pain_with_anhidrosis
dbr
:Lafora_disease
dbr
:Ornithine_aminotransferase_deficiency
dbr
:Ornithine_translocase_deficiency
dbr
:Otospondylomegaepiphyseal_dysplasia
dbr
:Antley–Bixler_syndrome
dbr
:Batten_disease
dbr
:Berdon_syndrome
dbr
:Bernard–Soulier_syndrome
dbr
:Lecithin_cholesterol_acyltransferase_deficiency
dbr
:Smith–Lemli–Opitz_syndrome
dbr
:Compound_heterozygosity
dbr
:Zunich–Kaye_syndrome
dbr
:Fatty-acid_metabolism_disorder
dbr
:Fraser_syndrome
dbr
:Friedreich's_ataxia
dbr
:Fucosidosis
dbr
:Fumarase_deficiency
dbr
:Harding_ataxia
dbr
:Keutel_syndrome
dbr
:Papillon–Lefèvre_syndrome
dbr
:Sugarman_syndrome
dbr
:Microspherophakia
dbr
:Microvillous_inclusion_disease
dbr
:Trimethylaminuria
dbr
:2-Hydroxyglutaric_aciduria
dbr
:6-Pyruvoyltetrahydropterin_synthase_deficiency
dbr
:Acute_fatty_liver_of_pregnancy
dbr
:Adducted_thumb_syndrome
dbr
:Adenine_phosphoribosyltransferase_deficiency
dbr
:Adenosine_deaminase_deficiency
dbr
:Adenylosuccinate_lyase_deficiency
dbr
:Trichothiodystrophy
dbr
:Tyrosinemia_type_II
dbr
:Wilson's_disease
dbr
:Distal_spinal_muscular_atrophy_type_1
dbr
:Dubin–Johnson_syndrome
dbr
:Dubowitz_syndrome
dbr
:GAPO_syndrome
dbr
:GM2-gangliosidosis,_AB_variant
dbr
:Galactokinase_deficiency
dbr
:Galactose-1-phosphate_uridylyltransferase_deficiency
dbr
:Galactosialidosis
dbr
:Galloway_Mowat_syndrome
dbr
:Gangliosidosis
dbr
:Gitelman_syndrome
dbr
:Cranio–lenticulo–sutural_dysplasia
dbr
:Hartnup_disease
dbr
:Juvenile_primary_lateral_sclerosis
dbr
:Lamellar_ichthyosis
dbr
:Laurence–Moon_syndrome
dbr
:Lipoid_congenital_adrenal_hyperplasia
dbr
:Long-chain_3-hydroxyacyl-coenzyme_A_dehydrogenase_deficiency
dbr
:Kostmann_syndrome
dbr
:Urofacial_syndrome
dbr
:Sabinas_brittle_hair_syndrome
dbr
:3-Methylcrotonyl-CoA_carboxylase_deficiency
dbr
:Acatalasia
dbr
:Acrocallosal_syndrome
dbr
:Aminoacylase_1_deficiency
dbr
:3C_syndrome
dbr
:Cystinosis
dbr
:EAST_syndrome
dbr
:Alpha-mannosidosis
dbr
:Familial_Mediterranean_fever
dbr
:Familial_isolated_vitamin_E_deficiency
dbr
:Fanconi_anemia
dbr
:Niemann–Pick_disease
dbr
:Niemann–Pick_disease,_SMPD1-associated
dbr
:Niemann–Pick_disease,_type_C
dbr
:Palmoplantar_keratoderma
dbr
:Carbamoyl_phosphate_synthetase_I_deficiency
dbr
:Cenani–Lenz_syndactylism
dbr
:Chronic_progressive_external_ophthalmoplegia
dbr
:Chédiak–Higashi_syndrome
dbr
:Diastrophic_dysplasia
dbr
:Dicarboxylic_aminoaciduria
dbr
:Dihydropyrimidine_dehydrogenase_deficiency
dbr
:Familial_dysautonomia
dbr
:Farber_disease
dbr
:Follicle-stimulating_hormone_insensitivity
dbr
:Fountain_syndrome
dbr
:Gerodermia_osteodysplastica
dbr
:Glucose-galactose_malabsorption
dbr
:Glutaric_acidemia_type_2
dbr
:Glutaric_aciduria_type_1
dbr
:Glutathione_synthetase_deficiency
dbr
:Glycine_encephalopathy
dbr
:Glycogen_storage_disease_type_V
dbr
:Gonadotropin-releasing_hormone_insensitivity
dbr
:Histidinemia
dbr
:Isobutyryl-coenzyme_A_dehydrogenase_deficiency
dbr
:Isolated_17,20-lyase_deficiency
dbr
:Isovaleric_acidemia
dbr
:Kapur–Toriello_syndrome
dbr
:Kaufman_oculocerebrofacial_syndrome
dbr
:Kohlschütter-Tönz_syndrome
dbr
:Restrictive_dermopathy
dbr
:Lucey–Driscoll_syndrome
dbr
:Rabson–Mendenhall_syndrome
dbr
:Refsum_disease
dbr
:2-Methylbutyryl-CoA_dehydrogenase_deficiency
dbr
:Griscelli_syndrome
dbr
:Guanidinoacetate_methyltransferase_deficiency
dbr
:Harlequin-type_ichthyosis
dbr
:Hemophagocytic_lymphohistiocytosis
dbr
:Hermansky–Pudlak_syndrome
dbr
:Atelosteogenesis,_type_II
dbr
:Atransferrinemia
dbr
:Jansky–Bielschowsky_disease
dbr
:Tangier_disease
dbr
:Tay–Sachs_disease
dbr
:Craniodiaphyseal_dysplasia
dbr
:Hurler_syndrome
dbr
:Hyperlysinemia
dbr
:Hypermethioninemia
dbr
:Hyperprolinemia
dbr
:Hypertryptophanemia
dbr
:Hypervalinemia
dbr
:Fish-eye_disease
dbr
:Marden–Walker_syndrome
dbr
:Young–Madders_syndrome
dbr
:Purine_nucleoside_phosphorylase_deficiency
dbr
:Very_long-chain_acyl-coenzyme_A_dehydrogenase_deficiency
dbr
:Argininemia
dbr
:Argininosuccinic_aciduria
dbr
:Abdallat–Davis–Farrage_syndrome
dbr
:Abderhalden–Kaufmann–Lignac_syndrome
dbr
:Ablepharon_macrostomia_syndrome
dbr
:Aceruloplasminemia
dbr
:Acheiropodia
dbr
:Acrodermatitis_enteropathica
dbr
:Chorea_acanthocytosis
dbr
:Aldolase_A_deficiency
dbr
:Kindler_syndrome
dbr
:Laron_syndrome
dbr
:Bietti's_crystalline_dystrophy
dbr
:Bloom_syndrome
dbr
:Blue_diaper_syndrome
dbr
:Hereditary_pyropoikilocytosis
dbr
:Holocarboxylase_synthetase_deficiency
dbr
:Wolman_disease
dbr
:Mismatch_repair_cancer_syndrome
dbr
:Mitochondrial_neurogastrointestinal_encephalopathy_syndrome
dbr
:Idiopathic_infantile_arterial_calcification
dbr
:Rapadilino_syndrome
dbr
:Triple-A_syndrome
dbr
:Arterial_tortuosity_syndrome
dbr
:Aspartylglucosaminuria
dbr
:Autosomal_recessive_multiple_epiphyseal_dysplasia
dbr
:CAMFAK_syndrome
dbr
:Pipecolic_acidemia
dbr
:Spinal_muscular_atrophy
dbr
:Fibrochondrogenesis
dbr
:Infantile_free_sialic_acid_storage_disease
dbr
:Krabbe_disease
dbr
:Methemoglobinemia
dbr
:Methylmalonic_acidemia
dbr
:Michels_syndrome
dbr
:Micro_syndrome
dbr
:Nemaline_myopathy
dbr
:Nezelof_syndrome
dbr
:Ataxia_telangiectasia
dbr
:Oculocutaneous_albinism
dbr
:Orotic_aciduria
dbr
:Canavan_disease
dbr
:Carnitine-acylcarnitine_translocase_deficiency
dbr
:Carnitine_palmitoyltransferase_I_deficiency
dbr
:Carnosinemia
dbr
:Carpenter_syndrome
dbr
:Cerebrotendineous_xanthomatosis
dbr
:Senior–Løken_syndrome
dbr
:Pseudo-Hurler_polydystrophy
dbr
:Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency
dbr
:Mevalonate_kinase_deficiency
dbr
:Mitochondrial_trifunctional_protein_deficiency
dbr
:Multiple_sulfatase_deficiency
dbr
:Unverricht–Lundborg_disease
dbr
:Rothmund–Thomson_syndrome
dbr
:Rotor_syndrome
dbr
:Spondylo-meta-epiphyseal_dysplasia
dbr
:Situs_inversus
dbr
:Sly_syndrome
dbr
:Urbach–Wiethe_disease
dbr
:Werner_syndrome
dbr
:Yunis–Varon_syndrome
dbr
:Netherton_syndrome
dbr
:Short-chain_acyl-coenzyme_A_dehydrogenase_deficiency
dbr
:Urocanic_aciduria
dbr
:Walker–Warburg_syndrome
dbr
:Ethylmalonic_encephalopathy
dbr
:Gunther_disease
dbr
:Iminoglycinuria
dbr
:Immunodeficiency–centromeric_instability–facial_anomalies_syndrome
dbr
:Lysinuric_protein_intolerance
dbr
:Lysosomal_acid_lipase_deficiency
dbr
:Oculodentodigital_dysplasia
dbr
:Oguchi_disease
dbr
:Triosephosphate_isomerase_deficiency
dbr
:Wiedemann–Rautenstrauch_syndrome
dbr
:Finnish_heritage_disease
dbr
:Giant_axonal_neuropathy
dbr
:Malonyl-CoA_decarboxylase_deficiency
dbr
:Malpuech_facial_clefting_syndrome
dbr
:Management_of_thalassemia
dbr
:Opsismodysplasia
dbr
:N-Acetylglutamate_synthase_deficiency
dbr
:Nakajo_syndrome
dbr
:Sickle_cell_trait
dbr
:Salla_disease
dbr
:Mucolipidosis
dbr
:Mucolipidosis_type_IV
dbr
:Mulibrey_nanism
dbr
:Zamzam–Sheriff–Phillips_syndrome
dbr
:Phosphofructokinase_deficiency
dbr
:Pontocerebellar_hypoplasia
dbr
:Shwachman–Diamond_syndrome
dbr
:Tyrosinemia_type_III
dbr
:Weissenbacher–Zweymüller_syndrome
dbr
:Cholesteryl_ester_storage_disease
dbr
:Type_I_tyrosinemia
dbr
:Raine_syndrome
dbr
:Reproductive_compensation
dbr
:Renal_dysplasia-limb_defects_syndrome
dbr
:Impossible_syndrome
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