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About:
http://dbpedia.org/class/yago/Abnormality114501726
An Entity of Type:
Thing
,
from Named Graph:
http://dbpedia.org
,
within Data Space:
dbpedia.org:8891
Property
Value
rdfs:
subClassOf
yago
:PhysicalCondition114034177
owl:
equivalentClass
yago-res
:wordnet_abnormality_114501726
owl:
sameAs
yago
:Abnormality114501726
is
rdf:
type
of
dbr
:Carnitine_palmitoyltransferase_II_deficiency
dbr
:Caroli_disease
dbr
:Cartilage–hair_hypoplasia
dbr
:Amelia_(birth_defect)
dbr
:Amelogenesis_imperfecta
dbr
:46,_XX/XY
dbr
:48,_XXXX
dbr
:49,_XXXXX
dbr
:49,_XXXXY_syndrome
dbr
:Becker's_nevus
dbr
:Beckwith–Wiedemann_syndrome
dbr
:Beholder_(Dungeons_&_Dragons)
dbr
:Benign_neonatal_hemangiomatosis
dbr
:Prader–Willi_syndrome
dbr
:Preauricular_sinus_and_cyst
dbr
:Primary_ciliary_dyskinesia
dbr
:Proboscis_(anomaly)
dbr
:Proteus_syndrome
dbr
:Prune_belly_syndrome
dbr
:Pseudoxanthoma_elasticum
dbr
:Ptosis_(eyelid)
dbr
:Pulmonary_hypoplasia
dbr
:Pulmonary_sequestration
dbr
:Pure_red_cell_aplasia
dbr
:Rubinstein–Taybi_syndrome
dbr
:Elastosis_perforans_serpiginosa
dbr
:Enteric_duplication_cyst
dbr
:Entropion
dbr
:Epidermolysis_bullosa
dbr
:Epidermolysis_bullosa_dystrophica
dbr
:Epidermolytic_hyperkeratosis
dbr
:Facial_cleft
dbr
:MOMO_syndrome
dbr
:Muckle–Wells_syndrome
dbr
:Nijmegen_breakage_syndrome
dbr
:MORM_syndrome
dbr
:MURCS_association
dbr
:Megalencephaly
dbr
:Megalocornea
dbr
:Megaureter
dbr
:Melanotic_neuroectodermal_tumor_of_infancy
dbr
:Membranous_aplasia_cutis
dbr
:Memory_leak
dbr
:Meningohydroencephalocoele
dbr
:Monosomy_14
dbr
:Monosomy_9p
dbr
:Monstrous_birth
dbr
:Nephronophthisis
dbr
:Persistent_Müllerian_duct_syndrome
dbr
:Propulsive_gait
dbr
:Parkinsonian_gait
dbr
:Smith–Magenis_syndrome
dbr
:Preureteric_vena_cava
dbr
:Saethre–Chotzen_syndrome
dbr
:Branchial_cleft_cyst
dbr
:Annular_pancreas
dbr
:Anomalous_pulmonary_venous_connection
dbr
:Anomaly_(physics)
dbr
:Anomaly_matching_condition
dbr
:Anophthalmia
dbr
:Anorchia
dbr
:Anotia
dbr
:Antalgic_gait
dbr
:Anterior_segment_mesenchymal_dysgenesis
dbr
:Apert_syndrome
dbr
:Aphalangia
dbr
:Aphallia
dbr
:Aplasia_cutis_congenita
dbr
:Arachnodactyly
dbr
:Arachnoid_cyst
dbr
:Arcuate_uterus
dbr
:Holt–Oram_syndrome
dbr
:Homocystinuria
dbr
:Horseshoe_kidney
dbr
:Hydranencephaly
dbr
:Hyperdontia
dbr
:Hypohidrotic_ectodermal_dysplasia
dbr
:Hypopituitarism
dbr
:Bhaskar–Jagannathan_syndrome
dbr
:Patau_syndrome
dbr
:Pectus_carinatum
dbr
:Peutz–Jeghers_syndrome
dbr
:Renal-hepatic-pancreatic_dysplasia
dbr
:Rigoletto
dbr
:Cubitus_valgus
dbr
:Cubitus_varus
dbr
:Currarino_syndrome
dbr
:Cutis_marmorata_telangiectatica_congenita
dbr
:Cutis_rhomboidalis_nuchae
dbr
:Cystic_eyeball
dbr
:Cystic_hygroma
dbr
:Dacryocystocele
dbr
:Dactyly
dbr
:Undefined_value
dbr
:Unibrow
dbr
:Usher_syndrome
dbr
:Van_der_Woude_syndrome
dbr
:Von_Hippel–Lindau_disease
dbr
:Dead_code
dbr
:Dead_store
dbr
:Donohue_syndrome
dbr
:Down_syndrome
dbr
:Dyschromia
dbr
:Dysmelia
dbr
:Dysostosis
dbr
:Easter_egg_(media)
dbr
:Incontinentia_pigmenti_achromians
dbr
:Infant_respiratory_distress_syndrome
dbr
:Iniencephaly
dbr
:Instanton
dbr
:Interrupt_storm
dbr
:Intersex
dbr
:Intestinal_malrotation
dbr
:Intrauterine_epidermal_necrosis
dbr
:Intrauterine_growth_restriction
dbr
:Intraventricular_hemorrhage
dbr
:Jacobsen_syndrome
dbr
:Johanson–Blizzard_syndrome
dbr
:Kursk_Magnetic_Anomaly
dbr
:Kvikk_case
dbr
:Musculoskeletal_abnormality
dbr
:Leukocyte_adhesion_deficiency
dbr
:Leukocyte_adhesion_deficiency-1
dbr
:Levocardia
dbr
:Limb–mammary_syndrome
dbr
:Paasselkä_devils
dbr
:Ponseti_method
dbr
:Rosenthal–Kloepfer_syndrome
dbr
:Skin_dimple
dbr
:Peccei–Quinn_theory
dbr
:Pelvic_digit
dbr
:Pendred_syndrome
dbr
:Pentalogy_of_Cantrell
dbr
:Potocki–Lupski_syndrome
dbr
:XXYY_syndrome
dbr
:Uterine_septum
dbr
:Wrinkly_skin_syndrome
dbr
:17q21.31_microdeletion_syndrome
dbr
:Congenital_diaphragmatic_hernia
dbr
:Congenital_insensitivity_to_pain
dbr
:Congenital_lacrimal_duct_obstruction
dbr
:Congenital_pulmonary_airway_malformation
dbr
:Cowden_syndrome
dbr
:Crandall_syndrome
dbr
:Craniosynostosis
dbr
:Crouzon_syndrome
dbr
:Cryptotia
dbr
:Amyoplasia
dbr
:Anaphase_lag
dbr
:Anodontia
dbr
:Meckel's_diverticulum
dbr
:Meckel_syndrome
dbr
:Esophageal_web
dbr
:Gastric_atresia
dbr
:Gauge_anomaly
dbr
:Gene_duplication
dbr
:Genodermatosis
dbr
:Low-set_ears
dbr
:Lowry–MacLean_syndrome
dbr
:Norrie_disease
dbr
:Occipital_horn_syndrome
dbr
:Ondine's_curse
dbr
:Ortolani_test
dbr
:Midline_cervical_cleft
dbr
:Thumb_hypoplasia
dbr
:Vaginal_atresia
dbr
:Steppage_gait
dbr
:Otocephaly
dbr
:Pallister–Killian_syndrome
dbr
:Simpson–Golabi–Behmel_syndrome
dbr
:Software_aging
dbr
:Vestigial_twin
dbr
:PHACES_Syndrome
dbr
:Perforating_calcific_elastosis
dbr
:Vici_syndrome
dbr
:Omphalomesenteric_duct_cyst
dbr
:Renal_agenesis
dbr
:Symmastia
dbr
:Urachus
dbr
:Tracheoesophageal_fistula
dbr
:Cystic_lymphatic_malformation
dbr
:Ullrich_disease
dbr
:18p-
dbr
:Chromosome_5q_deletion_syndrome
dbr
:Chronic_granulomatous_disease
dbr
:Ehlers–Danlos_syndrome
dbr
:Endocardial_fibroelastosis
dbr
:Epidermolysis_bullosa_simplex
dbr
:Gastroschisis
dbr
:Glitching
dbr
:Glycogen_storage_disease_type_I
dbr
:Brachymetatarsia
dbr
:Mondini_dysplasia
dbr
:Nager_acrofacial_dysostosis
dbr
:Nail–patella_syndrome
dbr
:Concha_bullosa
dbr
:Conformal_anomaly
dbr
:Congenital_absence_of_the_vas_deferens
dbr
:Congenital_amputation
dbr
:Congenital_cartilaginous_rest_of_the_neck
dbr
:Congenital_clasped_thumb
dbr
:Congenital_disorder_of_glycosylation_type_IIc
dbr
:Congenital_estrogen_deficiency
dbr
:Congenital_fiber_type_disproportion
dbr
:Congenital_hyperinsulinism
dbr
:Congenital_hypertrophy_of_the_lateral_fold_of_the_hallux
dbr
:Congenital_hypothyroidism
dbr
:Congenital_ichthyosiform_erythroderma
dbr
:Congenital_limb_deformities
dbr
:Congenital_lip_pit
dbr
:Congenital_malformations_of_the_dermatoglyphs
dbr
:Congenital_myasthenic_syndrome
dbr
:Congenital_rubella_syndrome
dbr
:Congenital_smooth_muscle_hamartoma
dbr
:Congenital_trigger_thumb
dbr
:Conjoined_twins
dbr
:Constriction_ring_syndrome
dbr
:Contiguous_gene_syndrome
dbr
:Cryopyrin-associated_periodic_syndrome
dbr
:Cryptophthalmos
dbr
:Labial_fusion
dbr
:Marshall–Smith_syndrome
dbr
:Platybasia
dbr
:Proximal_18q-
dbr
:Radial_dysplasia
dbr
:Sotos_syndrome
dbr
:True_hermaphroditism
dbr
:Unreachable_code
dbr
:Velamentous_cord_insertion
dbr
:Osteochondrodysplasia
dbr
:Osteochondroprogenitor_cell
dbr
:Otofacial_syndrome
dbr
:Pseudovaginal_perineoscrotal_hypospadias
dbr
:Androgen_insensitivity_syndrome
dbr
:Angelman_syndrome
dbr
:Aniridia
dbr
:Anonychia
dbr
:Aposthia
dbr
:Benjamin_syndrome
dbr
:Linear_focal_elastosis
dbr
:Lissencephaly
dbr
:List_of_Advanced_Dungeons_&_Dragons_2nd_edition_monsters
dbr
:Loeys–Dietz_syndrome
dbr
:Macrognathism
dbr
:Bochdalek_hernia
dbr
:Choanal_atresia
dbr
:Sinus_pericranii
dbr
:Sitosterolemia
dbr
:Smith–Lemli–Opitz_syndrome
dbr
:Cleft_palate_incidence_by_population
dbr
:Cleidocranial_dysostosis
dbr
:Clitoromegaly
dbr
:Cloacal_exstrophy
dbr
:Coloboma
dbr
:Coloboma_of_optic_nerve
dbr
:Colpocephaly
dbr
:Common_Weakness_Enumeration
dbr
:Deletion_(genetics)
dbr
:Denis_Browne_bar
dbr
:Dent's_disease
dbr
:Dentin_dysplasia
dbr
:Dentinogenesis_imperfecta
dbr
:Zadik–Barak–Levin_syndrome
dbr
:Emanuel_syndrome
dbr
:Fault_(technology)
dbr
:Fault_tolerance
dbr
:Femur_fibula_ulna_syndrome
dbr
:Frontonasal_dysplasia
dbr
:Fujikawa_method
dbr
:Fundic_gland_polyposis
dbr
:Club_foot
dbr
:Hailey–Hailey_disease
dbr
:Hair_whorl
dbr
:Hajdu–Cheney_syndrome
dbr
:Hallermann–Streiff_syndrome
dbr
:Hallux_varus
dbr
:Hammer_toe
dbr
:Hemangiomatosis
dbr
:Hemifacial_microsomia
dbr
:Hemihydranencephaly
dbr
:Hemihypertrophy
dbr
:Hemolytic_disease_of_the_newborn
dbr
:Ichthyosis_vulgaris
dbr
:Idiosyncratic_drug_reaction
dbr
:Igor_(Young_Frankenstein)
dbr
:Igor_(character)
dbr
:Keratoglobus
dbr
:Keutel_syndrome
dbr
:Mean_anomaly
dbr
:Mixed_anomaly
dbr
:Parity_anomaly
dbr
:Uhl_anomaly
dbr
:POEMS_syndrome
dbr
:Pachyonychia_congenita
dbr
:Pancreas_divisum
dbr
:Papillon–Lefèvre_syndrome
dbr
:Patterson_syndrome
dbr
:Pectus_excavatum
dbr
:Persistent_pupillary_membrane
dbr
:Philadelphia_chromosome
is
rdfs:
subClassOf
of
yago
:WikicatChromosomalAbnormalities
yago
:Aberrance114503665
yago
:Abrachia114466258
yago
:Acardia114019296
yago
:Acephalia114019441
yago
:Acorea114021853
yago
:Acromicria114021936
yago
:Acromphalus114022068
yago
:Amastia114022369
yago
:Aneuploidy114022661
yago
:Anomaly114505821
yago
:Anorchism114022849
yago
:ArrestedDevelopment114503354
yago
:Asynclitism114049098
yago
:Atresia114049262
yago
:Atypicality114503060
yago
:Brachydactyly114092114
yago
:Cryptorchidy114092247
yago
:Cyclopia114503990
yago
:DeviatedSeptum114092925
yago
:Dextrocardia114093325
yago
:Dysplasia114365950
yago
:Ectrodactyly114093464
yago
:Erethism114093723
yago
:FetalDistress114093874
yago
:Gynecomastia114506020
yago
:Hepatomegaly114103180
yago
:HydatidMole114192942
yago
:Hydramnios114193202
yago
:Hydrocephalus114465768
yago
:Hypervitaminosis114198829
yago
:Hypospadias114198997
yago
:Infantilism114507787
yago
:Inversion114103785
yago
:Irritation114531392
yago
:Lagophthalmos114199146
yago
:Macrencephaly114152492
yago
:Macrocephaly114508974
yago
:MentalAbnormality114200301
yago
:Microbrachia114509219
yago
:Microcephaly114509299
yago
:Nanophthalmos114200418
yago
:Pachycheilia114509491
yago
:Palmature114331271
yago
:Phimosis114509583
yago
:Pneumothorax114149536
yago
:Progeria114468348
yago
:WikicatGaitAbnormalities
yago
:Retroversion114531598
yago
:Sequela114550614
yago
:SpinalCurvature114504889
yago
:Strabismus114557415
yago
:Subnormality114505667
yago
:Torticollis114557719
yago
:Transposition114103998
yago
:Varix114573713
yago
:WikicatAbnormalitiesOfDermalFibrousAndElasticTissue
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