About: http://dbpedia.org/class/yago/Imperfection114462666

Property	Value
rdfs:subClassOf	yago:State100024720
owl:equivalentClass	yago-res:wordnet_imperfection_114462666
is rdf:type of	dbr:Carnitine_palmitoyltransferase_II_deficiency dbr:Caroli_disease dbr:Cartilage–hair_hypoplasia dbr:Amelia_(birth_defect) dbr:Amelogenesis_imperfecta dbr:48,_XXXX dbr:Becker's_nevus 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:Ptosis_(eyelid) dbr:Pulmonary_atresia dbr:Pulmonary_hypoplasia dbr:Pulmonary_sequestration dbr:Pure_red_cell_aplasia dbr:Rubinstein–Taybi_syndrome dbr:Schottky_defect dbr:Electromigration dbr:Elejalde_syndrome dbr:Enteric_duplication_cyst dbr:Entropion dbr:Epidermolysis_bullosa dbr:Epidermolysis_bullosa_dystrophica dbr:Epidermolytic_hyperkeratosis dbr:F-Center dbr:Facial_cleft dbr:MOMO_syndrome dbr:Muckle–Wells_syndrome dbr:Negative-bias_temperature_instability dbr:Nijmegen_breakage_syndrome dbr:Nitrogen-vacancy_center dbr:MORM_syndrome dbr:MURCS_association dbr:Megalencephaly dbr:Megalocornea dbr:Megaureter dbr:Melanotic_neuroectodermal_tumor_of_infancy dbr:Membranous_aplasia_cutis dbr:Meningohydroencephalocoele dbr:Metachondromatosis dbr:Monstrous_birth dbr:Nephronophthisis dbr:Persistent_Müllerian_duct_syndrome dbr:Preureteric_vena_cava dbr:Saethre–Chotzen_syndrome dbr:Branchial_cleft_cyst dbr:Annular_pancreas dbr:Anomalous_left_coronary_artery_from_the_pulmonary_artery dbr:Anomalous_pulmonary_venous_connection dbr:Anophthalmia dbr:Anorchia dbr:Anotia dbr:Anterior_segment_mesenchymal_dysgenesis dbr:Apert_syndrome dbr:Aphalangia dbr:Aphallia dbr:Aplasia_cutis_congenita dbr:Arachnodactyly dbr:Arachnoid_cyst dbr:Architectural_acoustics dbr:Arcuate_uterus dbr:Holt–Oram_syndrome dbr:Horseshoe_kidney dbr:Hydranencephaly dbr:Hyperdontia dbr:Hypohidrotic_ectodermal_dysplasia dbr:Hypophosphatasia dbr:Hypopituitarism dbr:Bhaskar–Jagannathan_syndrome dbr:Patau_syndrome dbr:Pectus_carinatum dbr:Pelger–Huet_anomaly dbr:Peutz–Jeghers_syndrome dbr:Renal-hepatic-pancreatic_dysplasia dbr:Cubitus_valgus dbr:Cubitus_varus dbr:Currarino_syndrome dbr:Current_crowding dbr:Cutis_marmorata_telangiectatica_congenita dbr:Cystic_eyeball dbr:Cystic_hygroma dbr:Dacryocystocele dbr:Dactyly dbr:Unibrow dbr:Usher_syndrome dbr:Van_der_Woude_syndrome dbr:Von_Hippel–Lindau_disease dbr:Donohue_syndrome dbr:Double_aortic_arch dbr:Down_syndrome dbr:Dyschromia dbr:Dysmelia dbr:Dysostosis dbr:Incontinentia_pigmenti_achromians dbr:Infant_respiratory_distress_syndrome dbr:Iniencephaly dbr:Intersex dbr:Interstitial_condensation dbr:Interstitial_defect dbr:Intestinal_malrotation dbr:Intrauterine_epidermal_necrosis dbr:Intrauterine_growth_restriction dbr:Intraventricular_hemorrhage dbr:Jacobsen_syndrome dbr:Johanson–Blizzard_syndrome dbr:Kvikk_case dbr:Settlement_(structural) dbr:Musculoskeletal_abnormality dbr:Leukocyte_adhesion_deficiency dbr:Leukocyte_adhesion_deficiency-1 dbr:Levocardia dbr:Limb–mammary_syndrome dbr:Ponseti_method dbr:Rosenthal–Kloepfer_syndrome dbr:Skin_dimple dbr:Persistent_left_superior_vena_cava dbr:Peierls_stress dbr:Pelvic_digit dbr:Pendred_syndrome dbr:Pentalogy_of_Cantrell dbr:Potocki–Lupski_syndrome dbr:Uterine_septum dbr:Congenital_diaphragmatic_hernia dbr:Congenital_insensitivity_to_pain dbr:Congenital_lacrimal_duct_obstruction dbr:Congenital_pulmonary_airway_malformation dbr:Cortisone_reductase_deficiency dbr:Cowden_syndrome dbr:Crandall_syndrome dbr:Craniosynostosis dbr:Crouzon_syndrome dbr:Cryptotia dbr:Amyoplasia dbr:Anodontia dbr:Meckel's_diverticulum dbr:Meckel_syndrome dbr:Esophageal_web dbr:Gastric_atresia dbr:Genodermatosis dbr:Low-set_ears dbr:Lowry–MacLean_syndrome dbr:Norrie_disease dbr:Ondine's_curse dbr:Ortolani_test dbr:Midline_cervical_cleft dbr:Thumb_hypoplasia dbr:Vaginal_atresia dbr:Otocephaly dbr:Simpson–Golabi–Behmel_syndrome dbr:Vestigial_twin dbr:PHACES_Syndrome dbr:Vici_syndrome dbr:Omphalomesenteric_duct_cyst dbr:Renal_agenesis dbr:Symmastia dbr:Thermal_bridge dbr:Urachus dbr:Tracheoesophageal_fistula dbr:RASopathy dbr:Cystic_lymphatic_malformation dbr:Chronic_granulomatous_disease dbr:Chronic_mucocutaneous_candidiasis dbr:Ehlers–Danlos_syndrome dbr:Endocardial_fibroelastosis dbr:Epidermodysplasia_verruciformis dbr:Epidermolysis_bullosa_simplex dbr:Frenkel_defect dbr:Gastroschisis dbr:Glossary_of_video_game_terms dbr:Glycogen_storage_disease_type_I dbr:Brachymetatarsia dbr:Mold_health_issues dbr:Mondini_dysplasia dbr:Nager_acrofacial_dysostosis dbr:Nail–patella_syndrome dbr:Concha_bullosa dbr:Congenital_absence_of_the_vas_deferens dbr:Congenital_amputation dbr:Congenital_cartilaginous_rest_of_the_neck dbr:Congenital_clasped_thumb dbr:Congenital_contractural_arachnodactyly 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_stenosis_of_vena_cava dbr:Congenital_trigger_thumb dbr:Conjoined_twins dbr:Constriction_ring_syndrome dbr:Corrupted_Blood_incident dbr:Cryopyrin-associated_periodic_syndrome dbr:Cryptophthalmos dbr:Crystallographic_defect dbr:Crystallographic_defects_in_diamond dbr:Damp_(structural) dbr:Labial_fusion dbr:Marshall–Smith_syndrome dbr:Platybasia dbr:SILC_(semiconductors) dbr:Radial_dysplasia dbr:Sotos_syndrome dbr:True_hermaphroditism dbr:Velamentous_cord_insertion dbr:Osteochondrodysplasia dbr:Osteochondroprogenitor_cell dbr:Osteopoikilosis dbr:Otofacial_syndrome dbr:Pseudovaginal_perineoscrotal_hypospadias dbr:Androgen_insensitivity_syndrome dbr:Aneurysm_of_sinus_of_Valsalva dbr:Aniridia dbr:Anonychia dbr:Aposthia dbr:Benjamin_syndrome dbr:Lissencephaly dbr:Macrognathism dbr:Bochdalek_hernia dbr:Choanal_atresia dbr:Sick_building_syndrome dbr:Sinus_pericranii dbr:Sitosterolemia dbr:Smith–Lemli–Opitz_syndrome dbr:Steatocystoma_multiplex dbr:Cleft_palate_incidence_by_population dbr:Cleidocranial_dysostosis dbr:Clitoromegaly dbr:Cloacal_exstrophy dbr:Coloboma dbr:Coloboma_of_optic_nerve dbr:Colpocephaly dbr:Denis_Browne_bar dbr:Dent's_disease dbr:Dentin_dysplasia dbr:Dentinogenesis_imperfecta dbr:Zadik–Barak–Levin_syndrome dbr:Fechtner_syndrome dbr:Feedback-controlled_electromigration dbr:Femur_fibula_ulna_syndrome dbr:Frontonasal_dysplasia dbr:Fundic_gland_polyposis dbr:Club_foot dbr:Haemophilia_A 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_bullosa_of_Siemens dbr:Ichthyosis_vulgaris dbr:Idiosyncratic_drug_reaction dbr:Keratin_disease dbr:Keratoglobus dbr:Keutel_syndrome 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:Piebaldism dbr:Pierre_Robin_syndrome dbr:Poland_syndrome dbr:Polymicrogyria dbr:Pulmonary_alveolar_proteinosis dbr:Macrocheilia dbr:Macrostomia dbr:Macrotia dbr:Sturge–Weber_syndrome dbr:Syrinx_(medicine) dbr:Tetralogy_of_Fallot dbr:Treacher_Collins_syndrome dbr:Maternal_autoimmune_bullous_disease dbr:May–Hegglin_anomaly dbr:McGillivray_syndrome dbr:Median_raphe_cyst dbr:Microcheilia dbr:Microcystic_lymphatic_malformation dbr:Microgenia dbr:Micrognathism
is rdfs:subClassOf of	yago:Defect114464005 yago:Defect114464203 yago:Defectiveness114472299 yago:Failing114462946 yago:Flaw114463170 yago:Wart114464883