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About:
clgr:
Ring_chromosome_20_syndrome
Property
Value
rdf:
type
owl:
NamedIndividual
Rare disease
Syndrome
Ring chromosome
Genetic disorder with no OMIM
rdfs:
label
Ring chromosome 20 syndrome
owl:
sameAs
dbr:
Ring_chromosome_20_syndrome
prov:
wasDerivedFrom
http://en.wikipedia.org/wiki/Category:Rare_diseases
http://en.wikipedia.org/wiki/Category:Syndromes
http://en.wikipedia.org/wiki/Category:Syndromes_by_affected_organ
http://en.wikipedia.org/wiki/Category:Syndromes_by_cause
http://en.wikipedia.org/wiki/List_of_syndromes
http://en.wikipedia.org/wiki/Category:Ring_chromosomes
http://en.wikipedia.org/wiki/Ring_chromosome
http://en.wikipedia.org/wiki/Category:Genetic_disorders_with_no_OMIM
skos:
prefLabel
Ring chromosome 20 syndrome
clgo:
icd10
Q93.2