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About:
clgr:
Trichothiodystrophy
Property
Value
rdf:
type
owl:
NamedIndividual
Rare disease
DNA replication and repair-deficiency disorder
Genodermatose
Autosomal recessive disorder
Congenital disorder
Progeroid syndrome
rdfs:
label
Trichothiodystrophy
owl:
sameAs
dbr:
Trichothiodystrophy
prov:
wasDerivedFrom
http://en.wikipedia.org/wiki/Category:Congenital_disorders
http://en.wikipedia.org/wiki/Category:DNA_replication_and_repair-deficiency_disorders
http://en.wikipedia.org/wiki/Category:Genodermatoses
http://en.wikipedia.org/wiki/DNA_repair
http://en.wikipedia.org/wiki/Category:Progeroid_syndromes
http://en.wikipedia.org/wiki/Category:Rare_diseases
http://en.wikipedia.org/wiki/List_of_diseases_(T)
http://en.wikipedia.org/wiki/List_of_syndromes
http://en.wikipedia.org/wiki/Ichthyosis
http://en.wikipedia.org/wiki/Cellular_senescence
http://en.wikipedia.org/wiki/List_of_congenital_disorders
http://en.wikipedia.org/wiki/Category:Autosomal_recessive_disorders
http://en.wikipedia.org/wiki/DNA_repair-deficiency_disorder
http://en.wikipedia.org/wiki/Progeroid_syndromes
skos:
prefLabel
Trichothiodystrophy
skos:
altLabel
Trichothiodystrophy (non-congenital forms)
trichothiodystrophy
clgo:
icd10
L67.8
clgo:
omim
234050
clgo:
orpha
33364
is
clgo:
differentialDiagnosis
of
Xeroderma pigmentosum