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About:
clgr:
Singleton_Merten_syndrome
Property
Value
rdf:
type
owl:
NamedIndividual
Autosomal dominant disorder
Rare syndrome
Primary immunodeficiency
Genetic disorder with no OMIM
rdfs:
label
Singleton Merten syndrome
owl:
sameAs
dbr:
Singleton_Merten_syndrome
prov:
wasDerivedFrom
http://en.wikipedia.org/wiki/List_of_primary_immunodeficiencies
http://en.wikipedia.org/wiki/Category:Autosomal_dominant_disorders
http://en.wikipedia.org/wiki/List_of_diseases_(S)
http://en.wikipedia.org/wiki/List_of_syndromes
http://en.wikipedia.org/wiki/Category:Rare_syndromes
http://en.wikipedia.org/wiki/Category:Genetic_disorders_with_no_OMIM
skos:
prefLabel
Singleton Merten syndrome
skos:
altLabel
Singleton-Merten syndrome
clgo:
icd10
Q78.8
clgo:
omim
182250
clgo:
orpha
85191