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About:
http://dbpedia.org/resource/Template:X-linked_disorders
An Entity of Type:
Thing
,
from Named Graph:
http://dbpedia.org
,
within Data Space:
dbpedia.org
Property
Value
dbo:
wikiPageID
18624665
(xsd:integer)
dbo:
wikiPageRevisionID
1066869251
(xsd:integer)
dbp:
wikiPageUsesTemplate
dbt
:Navbox
dbt
:Documentation
prov:
wasDerivedFrom
wikipedia-en
:Template:X-linked_disorders?oldid=1066869251&ns=10
is
dbp:
wikiPageUsesTemplate
of
dbr
:Amelogenesis_imperfecta
dbr
:Becker_muscular_dystrophy
dbr
:MASA_syndrome
dbr
:X-linked_spinal_muscular_atrophy_type_2
dbr
:Barth_syndrome
dbr
:Hypohidrotic_ectodermal_dysplasia
dbr
:L1_syndrome
dbr
:Pelizaeus–Merzbacher_disease
dbr
:Complete_androgen_insensitivity_syndrome
dbr
:Conradi–Hünermann_syndrome
dbr
:Menkes_disease
dbr
:Norrie_disease
dbr
:Occipital_horn_syndrome
dbr
:Simpson–Golabi–Behmel_syndrome
dbr
:Chronic_granulomatous_disease
dbr
:Emery–Dreifuss_muscular_dystrophy
dbr
:Androgen_insensitivity_syndrome
dbr
:Lesch–Nyhan_syndrome
dbr
:Choroideremia
dbr
:Sideroblastic_anemia
dbr
:Dent's_disease
dbr
:Haemophilia_A
dbr
:Haemophilia_B
dbr
:Ocular_albinism_type_1
dbr
:Centronuclear_myopathy
dbr
:Aicardi_syndrome
dbr
:Wiskott–Aldrich_syndrome
dbr
:X-linked_myotubular_myopathy
dbr
:Adrenoleukodystrophy
dbr
:Alport_syndrome
dbr
:Duchenne_muscular_dystrophy
dbr
:Dyskeratosis_congenita
dbr
:Partial_androgen_insensitivity_syndrome
dbr
:Danon_disease
dbr
:Focal_dermal_hypoplasia
dbr
:Fragile_X_syndrome
dbr
:Glucose-6-phosphate_dehydrogenase_deficiency
dbr
:Smith–Fineman–Myers_syndrome
dbr
:Rett_syndrome
dbr
:Craniofrontonasal_dysplasia
dbr
:Hunter_syndrome
dbr
:Hyper-IgM_syndrome_type_1
dbr
:ATR-X_syndrome
dbr
:Kallmann_syndrome
dbr
:Coffin–Lowry_syndrome
dbr
:X-linked_recessive_inheritance
dbr
:Diabetes_insipidus
dbr
:CHILD_syndrome
dbr
:Incontinentia_pigmenti
dbr
:Mild_androgen_insensitivity_syndrome
dbr
:Brunner_syndrome
dbr
:Nephrogenic_diabetes_insipidus
dbr
:Ocular_albinism
dbr
:X-linked_agammaglobulinemia
dbr
:X-linked_hypophosphatemia
dbr
:X-linked_lymphoproliferative_disease
dbr
:X-linked_severe_combined_immunodeficiency
dbr
:McLeod_syndrome
dbr
:Spinal_and_bulbar_muscular_atrophy
dbr
:FG_syndrome
dbr
:IPEX_syndrome
dbr
:Lujan–Fryns_syndrome
dbr
:Ornithine_transcarbamylase_deficiency
dbr
:Oculocerebrorenal_syndrome
dbr
:Nasodigitoacoustic_syndrome
dbr
:Mohr–Tranebjærg_syndrome
dbr
:X-linked_intellectual_disability
dbr
:X-linked_adrenal_hypoplasia_congenita
dbr
:X-linked_ichthyosis
dbr
:Orofaciodigital_syndrome_1
dbr
:Properdin_deficiency
dbr
:Sex_linkage
dbr
:X-linked_dominant_inheritance
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