Browse using
OpenLink Faceted Browser
OpenLink Structured Data Editor
LodLive Browser
Formats
RDF:
N-Triples
N3
Turtle
JSON
XML
OData:
Atom
JSON
Microdata:
JSON
HTML
Embedded:
JSON
Turtle
Other:
CSV
JSON-LD
Faceted Browser
Sparql Endpoint
About:
http://dbpedia.org/class/yago/WikicatCongenitalDisorders
An Entity of Type:
Thing
,
from Named Graph:
http://dbpedia.org
,
within Data Space:
dbpedia.org
Property
Value
rdfs:
subClassOf
yago
:BirthDefect114465048
owl:
equivalentClass
yago-res
:wikicat_Congenital_disorders
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
:Prader–Willi_syndrome
dbr
:Primary_ciliary_dyskinesia
dbr
:Proboscis_(anomaly)
dbr
:Proteus_syndrome
dbr
:Prune_belly_syndrome
dbr
:Ptosis_(eyelid)
dbr
:Pulmonary_sequestration
dbr
:Pure_red_cell_aplasia
dbr
:Rubinstein–Taybi_syndrome
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
:Megaureter
dbr
:Meningohydroencephalocoele
dbr
:Monstrous_birth
dbr
:Saethre–Chotzen_syndrome
dbr
:Branchial_cleft_cyst
dbr
:Annular_pancreas
dbr
:Anomalous_pulmonary_venous_connection
dbr
:Anophthalmia
dbr
:Anterior_segment_mesenchymal_dysgenesis
dbr
:Apert_syndrome
dbr
:Aplasia_cutis_congenita
dbr
:Arachnodactyly
dbr
:Arachnoid_cyst
dbr
:Holt–Oram_syndrome
dbr
:Horseshoe_kidney
dbr
:Hyperdontia
dbr
:Hypohidrotic_ectodermal_dysplasia
dbr
:Bhaskar–Jagannathan_syndrome
dbr
:Patau_syndrome
dbr
:Pectus_carinatum
dbr
:Peutz–Jeghers_syndrome
dbr
:Renal-hepatic-pancreatic_dysplasia
dbr
:Currarino_syndrome
dbr
:Cutis_marmorata_telangiectatica_congenita
dbr
:Cystic_hygroma
dbr
:Dacryocystocele
dbr
:Unibrow
dbr
:Usher_syndrome
dbr
:Van_der_Woude_syndrome
dbr
:Von_Hippel–Lindau_disease
dbr
:Donohue_syndrome
dbr
:Down_syndrome
dbr
:Dysmelia
dbr
:Incontinentia_pigmenti_achromians
dbr
:Infant_respiratory_distress_syndrome
dbr
:Iniencephaly
dbr
:Intersex
dbr
:Intestinal_malrotation
dbr
:Intrauterine_growth_restriction
dbr
:Intraventricular_hemorrhage
dbr
:Jacobsen_syndrome
dbr
:Kvikk_case
dbr
:Ponseti_method
dbr
:Pelvic_digit
dbr
:Pendred_syndrome
dbr
:Pentalogy_of_Cantrell
dbr
:Potocki–Lupski_syndrome
dbr
:Congenital_diaphragmatic_hernia
dbr
:Congenital_pulmonary_airway_malformation
dbr
:Cowden_syndrome
dbr
:Crandall_syndrome
dbr
:Craniosynostosis
dbr
:Crouzon_syndrome
dbr
:Amyoplasia
dbr
:Anodontia
dbr
:Meckel's_diverticulum
dbr
:Genodermatosis
dbr
:Ondine's_curse
dbr
:Thumb_hypoplasia
dbr
:Vaginal_atresia
dbr
:Simpson–Golabi–Behmel_syndrome
dbr
:Vestigial_twin
dbr
:Vici_syndrome
dbr
:Renal_agenesis
dbr
:Urachus
dbr
:Ehlers–Danlos_syndrome
dbr
:Endocardial_fibroelastosis
dbr
:Epidermolysis_bullosa_simplex
dbr
:Gastroschisis
dbr
:Glycogen_storage_disease_type_I
dbr
:Brachymetatarsia
dbr
:Mondini_dysplasia
dbr
:Nager_acrofacial_dysostosis
dbr
:Nail–patella_syndrome
dbr
:Concha_bullosa
dbr
:Congenital_absence_of_the_vas_deferens
dbr
:Congenital_fiber_type_disproportion
dbr
:Congenital_hyperinsulinism
dbr
:Congenital_hypothyroidism
dbr
:Congenital_ichthyosiform_erythroderma
dbr
:Congenital_myasthenic_syndrome
dbr
:Congenital_rubella_syndrome
dbr
:Conjoined_twins
dbr
:Constriction_ring_syndrome
dbr
:Cryopyrin-associated_periodic_syndrome
dbr
:Cryptophthalmos
dbr
:Labial_fusion
dbr
:Marshall–Smith_syndrome
dbr
:Radial_dysplasia
dbr
:Sotos_syndrome
dbr
:Velamentous_cord_insertion
dbr
:Osteochondrodysplasia
dbr
:Osteochondroprogenitor_cell
dbr
:Androgen_insensitivity_syndrome
dbr
:Aniridia
dbr
:Anonychia
dbr
:Benjamin_syndrome
dbr
:Lissencephaly
dbr
:Choanal_atresia
dbr
:Sitosterolemia
dbr
:Smith–Lemli–Opitz_syndrome
dbr
:Cleft_palate_incidence_by_population
dbr
:Clitoromegaly
dbr
:Cloacal_exstrophy
dbr
:Coloboma
dbr
:Coloboma_of_optic_nerve
dbr
:Colpocephaly
dbr
:Denis_Browne_bar
dbr
:Dentin_dysplasia
dbr
:Dentinogenesis_imperfecta
dbr
:Zadik–Barak–Levin_syndrome
dbr
:Femur_fibula_ulna_syndrome
dbr
:Club_foot
dbr
:Hailey–Hailey_disease
dbr
:Hair_whorl
dbr
:Hajdu–Cheney_syndrome
dbr
:Hallux_varus
dbr
:Hemifacial_microsomia
dbr
:Hemihypertrophy
dbr
:Hemolytic_disease_of_the_newborn
dbr
:Ichthyosis_vulgaris
dbr
:Idiosyncratic_drug_reaction
dbr
:Keutel_syndrome
dbr
:Uhl_anomaly
dbr
:POEMS_syndrome
dbr
:Pachyonychia_congenita
dbr
:Patterson_syndrome
dbr
:Pectus_excavatum
dbr
:Persistent_pupillary_membrane
dbr
:Piebaldism
dbr
:Poland_syndrome
dbr
:Polymicrogyria
dbr
:Macrocheilia
dbr
:Sturge–Weber_syndrome
dbr
:Tetralogy_of_Fallot
dbr
:Micrognathism
dbr
:Microstomia
dbr
:Multiple_abnormalities
dbr
:Potocki–Shaffer_syndrome
dbr
:Autoimmune_lymphoproliferative_syndrome
dbr
:Autosomal_dominant_polycystic_kidney_disease
dbr
:Ayazi_syndrome
dbr
:Agenesis_of_the_corpus_callosum
dbr
:Tracheobronchomalacia
dbr
:Tracheomalacia
dbr
:Trichothiodystrophy
dbr
:Tuberous_sclerosis
dbr
:Wiskott–Aldrich_syndrome
dbr
:Distichia
dbr
:Dolichostenomelia
dbr
:Dubowitz_syndrome
dbr
:Hartnup_disease
dbr
:Hearing_loss_with_craniofacial_syndromes
dbr
:Lamellar_ichthyosis
dbr
:Laryngeal_cleft
dbr
:Laryngomalacia
dbr
:Late_congenital_syphilitic_oculopathy
dbr
:Lisch_nodule
dbr
:Li–Fraumeni_syndrome
dbr
:Splenogonadal_fusion
dbr
:Rudiger_syndrome
dbr
:Urofacial_syndrome
dbr
:Shprintzen–Goldberg_syndrome
dbr
:Phrygian_cap_(anatomy)
dbr
:Acatalasia
dbr
:Achondrogenesis
dbr
:Alport_syndrome
dbr
:2q37_monosomy
dbr
:Dandy–Walker_syndrome
dbr
:Duane_syndrome
dbr
:Duodenal_atresia
dbr
:Ectopic_pancreas
dbr
:Esophageal_atresia
dbr
:Fibrodysplasia_ossificans_progressiva
dbr
:Flat_feet
dbr
:Angiomatosis
dbr
:Angiomyolipoma
dbr
:Ablepharon
dbr
:Bangstad_syndrome
dbr
:Barakat_syndrome
dbr
:Bardet–Biedl_syndrome
dbr
:Cardiofaciocutaneous_syndrome
dbr
:Caudal_regression_syndrome
dbr
:Cavernous_hemangioma
dbr
:Ciliopathy
dbr
:Diamond–Blackfan_anemia
dbr
:Diphallia
dbr
:Diprosopus
dbr
:Familial_male-limited_precocious_puberty
dbr
:Foix–Alajouanine_syndrome
dbr
:Germ_cell_tumor
dbr
:Glycogen_storage_disease_type_V
dbr
:Goldberg–Shprintzen_syndrome
dbr
:Goldenhar_syndrome
dbr
:Gonadal_dysgenesis
dbr
:Gray_matter_heterotopia
dbr
:Hip_dysplasia
dbr
:Hirschsprung's_disease
dbr
:Katz_syndrome
dbr
:Kaufman_oculocerebrofacial_syndrome
dbr
:Kniest_dysplasia
dbr
:Legius_syndrome
dbr
:Arnold–Chiari_malformation
dbr
:Persistent_cloaca
dbr
:Miller–Dieker_syndrome
dbr
:Smith–Fineman–Myers_syndrome
dbr
:Lucey–Driscoll_syndrome
dbr
:Potter_sequence
dbr
:1q21.1_copy_number_variations
dbr
:1q21.1_deletion_syndrome
dbr
:1q21.1_duplication_syndrome
dbr
:Halal_syndrome
dbr
:Harlequin-type_ichthyosis
dbr
:Hemifacial_hypertrophy
dbr
:Atransferrinemia
dbr
:Intestinal_atresia
dbr
:Intestinal_neuronal_dysplasia
dbr
:Craniodiaphyseal_dysplasia
dbr
:Cranioschisis
dbr
:Teratoma
dbr
:Hutchinson's_triad
dbr
:Hydrolethalus_syndrome
dbr
:Hydrops_fetalis
dbr
:Hypertelorism
dbr
:Hypochondroplasia
dbr
:Hypoplastic_left_heart_syndrome
dbr
:Hypotelorism
dbr
:Marden–Walker_syndrome
dbr
:Marfanoid
dbr
:Trisomy_22
dbr
:Arrhinia
dbr
:Arthrogryposis
dbr
:Asplenia
dbr
:Aagenaes_syndrome
dbr
:Aarskog–Scott_syndrome
dbr
:Ablepharon_macrostomia_syndrome
dbr
:Acalvaria
dbr
:Accessory_spleen
dbr
:Achondrogenesis_type_1B
dbr
:Achondrogenesis_type_2
dbr
:Acrania
dbr
:Acrodysostosis
dbr
:Choledochal_cysts
dbr
:Junctional_epidermolysis_bullosa_(medicine)
dbr
:Kallmann_syndrome
dbr
:Keratitis–ichthyosis–deafness_syndrome
dbr
:Langer_mesomelic_dysplasia
dbr
:Large_for_gestational_age
dbr
:Biliary_atresia
dbr
:Björnstad_syndrome
dbr
:Bladder_exstrophy
dbr
:Blaschko's_lines
dbr
:Blepharophimosis
dbr
:Bloom_syndrome
dbr
:Blount's_disease
dbr
:Blue_rubber_bleb_nevus_syndrome
dbr
:Syringomyelia
dbr
:Coarctation_of_the_aorta
dbr
:Cold_urticaria
dbr
:Ectodermal_dysplasia
dbr
:Ectopia_(medicine)
dbr
:Ectopia_cordis
dbr
:Edwards_syndrome
dbr
:Heterochromia_iridum
dbr
:Heterotopia_(medicine)
dbr
:Holocarboxylase_synthetase_deficiency
dbr
:Holoprosencephaly
dbr
:Tetrasomy_18p
dbr
:Tietz_syndrome
dbr
:Trevor_disease
dbr
:Worth_syndrome
dbr
:Zellweger_syndrome
dbr
:Trigonocephaly
dbr
:Refractive_error
This content was extracted from
Wikipedia
and is licensed under the
Creative Commons Attribution-ShareAlike 3.0 Unported License