About: X-linked recessive disorders

An Entity of Type: Concept, from Named Graph: http://dbpedia.org, within Data Space: dbpedia.org:8891

Property	Value
dbo:wikiPageID	27090049 (xsd:integer)
dbo:wikiPageRevisionID	829519064 (xsd:integer)
dbp:wikiPageUsesTemplate	dbt:Commonscat dbt:Cat_more
rdf:type	skos:Concept
rdfs:label	X-linked recessive disorders (en)
skos:broader	dbc:Genetic_disorders_by_inheritance
skos:prefLabel	X-linked recessive disorders (en)
prov:wasDerivedFrom	wikipedia-en:Category:X-linked_recessive_disorders?oldid=829519064&ns=14
owl:sameAs	dbc:X-linked_recessive_disorders
is dbo:wikiPageWikiLink of	dbr:Becker_muscular_dystrophy dbr:MASA_syndrome dbr:X-linked_spinal_muscular_atrophy_type_2 dbr:DDX3X_syndrome dbr:Early-onset_parkinsonism-intellectual_disability_syndrome dbr:L1_syndrome dbr:Pelizaeus–Merzbacher_disease dbr:Proud_syndrome dbr:Wieacker_syndrome dbr:Menkes_disease dbr:Norrie_disease dbr:Occipital_horn_syndrome dbr:Renpenning's_syndrome dbr:Simpson–Golabi–Behmel_syndrome dbr:XMEN_disease dbr:Endocardial_fibroelastosis dbr:Congenital_red–green_color_blindness dbr:Creatine_transporter_defect dbr:Oto-palato-digital_syndrome dbr:Color_blindness dbr:Haemophilia_A dbr:Haemophilia_B dbr:Ocular_albinism_type_1 dbr:Adrenoleukodystrophy dbr:Duchenne_muscular_dystrophy dbr:Fabry_disease dbr:Smith–Fineman–Myers_syndrome dbr:Haemophilia dbr:Aldred_syndrome dbr:X-linked_dystonia_parkinsonism dbr:Hoyeraal–Hreidarsson_syndrome dbr:Ocular_albinism dbr:X-linked_agammaglobulinemia dbr:McLeod_syndrome dbr:Spinal_and_bulbar_muscular_atrophy dbr:FG_syndrome dbr:Lysosomal_storage_disease dbr:Ornithine_transcarbamylase_deficiency dbr:Ocular_albinism_late_onset_sensorineural_deafness dbr:Oculocerebrorenal_syndrome dbr:Nasodigitoacoustic_syndrome dbr:Say–Meyer_syndrome dbr:Morse–Rawnsley–Sargent_syndrome dbr:X-linked_intellectual_disability dbr:X-linked_complicated_corpus_callosum_dysgenesis dbr:X-linked_sideroblastic_anemia_and_spinocerebellar_ataxia dbr:X-linked_recessive_chondrodysplasia_punctata dbr:Papillary_fibroelastoma
is dcterms:subject of	dbr:Becker_muscular_dystrophy dbr:MASA_syndrome dbr:X-linked_spinal_muscular_atrophy_type_2 dbr:DDX3X_syndrome dbr:Early-onset_parkinsonism-intellectual_disability_syndrome dbr:L1_syndrome dbr:Pelizaeus–Merzbacher_disease dbr:Proud_syndrome dbr:Wieacker_syndrome dbr:Menkes_disease dbr:Norrie_disease dbr:Occipital_horn_syndrome dbr:Renpenning's_syndrome dbr:Simpson–Golabi–Behmel_syndrome dbr:XMEN_disease dbr:Endocardial_fibroelastosis dbr:Congenital_red–green_color_blindness dbr:Creatine_transporter_defect dbr:Oto-palato-digital_syndrome dbr:Color_blindness dbr:Haemophilia_A dbr:Haemophilia_B dbr:Ocular_albinism_type_1 dbr:Adrenoleukodystrophy dbr:Duchenne_muscular_dystrophy dbr:Fabry_disease dbr:Smith–Fineman–Myers_syndrome dbr:Haemophilia dbr:Aldred_syndrome dbr:X-linked_dystonia_parkinsonism dbr:Hoyeraal–Hreidarsson_syndrome dbr:Ocular_albinism dbr:X-linked_agammaglobulinemia dbr:McLeod_syndrome dbr:Spinal_and_bulbar_muscular_atrophy dbr:FG_syndrome dbr:Lysosomal_storage_disease dbr:Ornithine_transcarbamylase_deficiency dbr:Ocular_albinism_late_onset_sensorineural_deafness dbr:Oculocerebrorenal_syndrome dbr:Nasodigitoacoustic_syndrome dbr:Say–Meyer_syndrome dbr:Morse–Rawnsley–Sargent_syndrome dbr:X-linked_intellectual_disability dbr:X-linked_complicated_corpus_callosum_dysgenesis dbr:X-linked_sideroblastic_anemia_and_spinocerebellar_ataxia dbr:X-linked_recessive_chondrodysplasia_punctata dbr:Papillary_fibroelastoma