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About:
Lujan–Fryns syndrome
An Entity of Type:
disease
,
from Named Graph:
http://dbpedia.org
,
within Data Space:
dbpedia-live.demo.openlinksw.com
Rare genetic condition in humans
Property
Value
dbo:
description
malattia genetica legata al cromosoma X
(it)
rare genetic condition in humans
(en)
dbo:
diseasesDB
32654
dbo:
geneReviewsId
NBK1676
dbo:
geneReviewsName
MED12-Related Disorders
(en)
dbo:
icd10
F70.1
dbo:
icd9
317
dbo:
medicalSpecialty
dbr
:Medical_genetics
dbo:
omim
309520
(xsd:integer)
dbo:
thumbnail
wiki-commons
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dbo:
wikiPageExternalLink
https://www.ncbi.nlm.nih.gov/books/NBK1676/
dbo:
wikiPageWikiLink
dbc
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dbr
:Coactivator_(genetics)
dbr
:Macrocephaly
dbr
:Hypoplasia
dbr
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dbr
:Sex_linkage
dbr
:MRNA_surveillance
dbr
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dbr
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dbr
:Hypotonia
dbr
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dbr
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dbr
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dbr
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dbc
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dbr
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dbr
:Sphincter
dbr
:Medical_genetics
dbr
:Cardiology
dbr
:Malnutrition
dbr
:Embryo
dbr
:Low_frustration_tolerance
dbr
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dbr
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dbr
:Human_eye
dbr
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dbr
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dbr
:Nonsense_mutation
dbr
:Soft_palate
dbr
:Ascending_aorta
dbr
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dbc
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dbr
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dbc
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dbr
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dbr
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dbr
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dbr
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dbr
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dbr
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dbr
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dbc
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dbr
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:Human_voice
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:Anorexia_(symptom)
dbc
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dbr
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dbr
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dbr
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dbr
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dbr
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dbr
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dbr
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dbr
:Asparagine
dbr
:Cell_type
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dbr
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dbr
:Female
dbr
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dbr
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dbr
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dbp:
caption
Lujan–Fryns syndrome in a young adult male, with features that include a long, narrow face and recessed chin.
(en)
dbp:
imageSize
300
(xsd:integer)
dbp:
name
Lujan–Fryns syndrome
(en)
dbp:
specialty
dbr
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dbp:
synonyms
X-linked mental retardation with Marfanoid habitus, Lujan syndrome
(en)
dbp:
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dbt
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dbt
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dct:
subject
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dbc
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dbc
:X-linked_dominant_disorders
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gold:
hypernym
dbr
:X'
rdf:
type
owl
:Thing
wikidata
:Q12136
dbo
:Disease
dbo
:Disease
rdfs:
label
Lujan–Fryns syndrome
(en)
متلازمة لوجان-فرينس
(ar)
Lujan-Fryns-Syndrom
(de)
Syndrome de Lujan-Fryns
(fr)
Sindrome di Lujan-Fryns
(it)
Zespół Lujana-Frynsa
(pl)
owl:
sameAs
freebase
:Lujan–Fryns syndrome
wikidata
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wikidata
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dbpedia-global
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dbr
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prov:
wasDerivedFrom
wikipedia-en
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foaf:
depiction
wiki-commons
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foaf:
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