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owl:sameAs
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asEquivalent
b3s
b3sifp
facets
http://www.w3.org/2002/07/owl#
ldp
oplweb
skos-trans
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About:
Ornithine Carbamoyltransferase Deficiency Disease
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An Entity of Type :
http://linked.opendata.cz/ontology/ndfrt/DiseaseOrFinding
, within Data Space :
linked.opendata.cz
associated with source
document(s)
Type:
http://linked.opendata.cz/ontology/ndfrt/DiseaseOrFinding
New Facet based on Instances of this Class
Attributes
Values
rdf:type
http://linked.opendata.cz/ontology/ndfrt/DiseaseOrFinding
Title
Ornithine Carbamoyltransferase Deficiency Disease
(en)
skos:broader
Genetic Diseases, X-Linked
Urea Cycle Disorders, Inborn
skos:prefLabel
Ornithine Carbamoyltransferase Deficiency Disease
(en)
adms:identifier
http://linked.opendata.cz/resource/ndfrt/disease/N0000004014/identifier/ndfrt/
http://linked.opendata.cz/resource/ndfrt/disease/N0000004014/identifier/ndfrt/N0000004014
http://linked.open...gy/ndfrt/UMLS_CUI
C0268542
skos:altLabel
Ornithine Transcarbamylase Deficiency, Hyperammonemia Due To
(en)
Deficiency Disease, Ornithine Carbamoyltransferase
(en)
Deficiency Disease, Ornithine Transcarbamylase
(en)
OTC Deficiency
(en)
Ornithine Carbamoyltransferase Deficiency
(en)
Ornithine Transcarbamylase Deficiency
(en)
Ornithine Transcarbamylase Deficiency Disease
(en)
http://linked.open.../ndfrt/SNOMED_CID
80908008
http://linked.open...gy/ndfrt/MeSH_DUI
D020163
Faceted Search & Find service v1.16.118 as of Jun 21 2024
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