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About:
Autosomal dominant disorders
An Entity of Type:
Concept
,
from Named Graph:
http://dbpedia.org
,
within Data Space:
dbpedia.org
Property
Value
dbo:
wikiPageID
27089987
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dbo:
wikiPageRevisionID
1062936589
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dbp:
wikiPageUsesTemplate
dbt
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dbt
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dbt
:Cat_main
rdf:
type
skos
:Concept
rdfs:
label
Autosomal dominant disorders
(en)
skos:
broader
dbc
:Genetic_disorders_by_inheritance
skos:
prefLabel
Autosomal dominant disorders
(en)
prov:
wasDerivedFrom
wikipedia-en
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is
dbo:
wikiPageWikiLink
of
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dbr
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dbr
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:Gardner's_syndrome
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:Roussy–Lévy_syndrome
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:Zori–Stalker–Williams_syndrome
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is
dcterms:
subject
of
dbr
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dbr
:Benign_hereditary_chorea
dbr
:Rubinstein–Taybi_syndrome
dbr
:MOMO_syndrome
dbr
:Multiple_endocrine_neoplasia
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:Metachondromatosis
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:Hyperinsulinism-hyperammonemia_syndrome
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:Hypertrophic_cardiomyopathy
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:Hypodysfibrinogenemia
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:Bethlem_myopathy
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:Pelger–Huët_anomaly
dbr
:Peutz–Jeghers_syndrome
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:Currarino_syndrome
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:Cyprus_facial_neuromusculoskeletal_syndrome
dbr
:Czech_dysplasia,_metatarsal_type
dbr
:Variegate_porphyria
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:Vitelliform_macular_dystrophy
dbr
:Von_Hippel–Lindau_disease
dbr
:Von_Willebrand_disease
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:Dysfibrinogenemia
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:Leucine-sensitive_hypoglycemia_of_infancy
dbr
:Liddle's_syndrome
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:Pseudoachondroplasia
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:Singleton_Merten_syndrome
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:Medullary_cystic_kidney_disease
dbr
:Menke-Hennekam_syndrome
dbr
:RASopathy
dbr
:Gardner's_syndrome
dbr
:Gillespie_syndrome
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:Brachydactyly-long_thumb_syndrome
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:Branchio-oto-renal_syndrome
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:Myotonic_dystrophy
dbr
:Nail–patella_syndrome
dbr
:Congenital_distal_spinal_muscular_atrophy
dbr
:Congenital_stromal_corneal_dystrophy
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:Marshall_syndrome
dbr
:Marsili_syndrome
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:Otofaciocervical_syndrome
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:Aromatase_excess_syndrome
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:Calvarial_doughnut_lesions-bone_fragility_syndrome
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:Coloboma_of_macula-brachydactyly_type_B_syndrome
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:Zori–Stalker–Williams_syndrome
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:Oculopharyngeal_muscular_dystrophy
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:St._Helena_familial_genu_valgum
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:Severe_intellectual_disability-progressive_spastic_diplegia_syndrome
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:Ventricular_extrasystoles_with_syncopa...s-perodactyly-Robin_sequence_syndrome
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:Pallister–Hall_syndrome
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:Palmoplantar_keratoderma_with_deafness
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:SYT1-associated_neurodevelopmental_disorder
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:Parastremmatic_dwarfism
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dbr
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is
skos:
broader
of
dbc
:Transcription_factor_deficiencies
dbc
:RASopathies
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