Omenn syndrome - CaLiGraph

CaLiGraph

Property	Value
rdf:type	owl:NamedIndividual Rare syndrome Skin condition Combined T and B–cell immunodeficiency Noninfectious immunodeficiency-related cutaneous condition Primary immunodeficiency Autosomal recessive disorder
rdfs:label	Omenn syndrome
owl:sameAs	dbr:Omenn_syndrome
prov:wasDerivedFrom	http://en.wikipedia.org/wiki/Category:Noninfectious_immunodeficiency-related_cutaneous_conditions http://en.wikipedia.org/wiki/List_of_primary_immunodeficiencies http://en.wikipedia.org/wiki/List_of_diseases_(O) http://en.wikipedia.org/wiki/List_of_skin_conditions http://en.wikipedia.org/wiki/List_of_syndromes http://en.wikipedia.org/wiki/RNase_MRP http://en.wikipedia.org/wiki/Eosinophilia http://en.wikipedia.org/wiki/Category:Combined_T_and_B%E2%80%93cell_immunodeficiencies http://en.wikipedia.org/wiki/Severe_combined_immunodeficiency http://en.wikipedia.org/wiki/Category:Rare_syndromes http://en.wikipedia.org/wiki/Category:Autosomal_recessive_disorders
skos:prefLabel	Omenn syndrome
clgo:diseasesDB	32676
clgo:eMedicineSubject	ped
clgo:eMedicineTopic	1640
clgo:icd10	D81.2 (ILDSD81.210)
clgo:omim	603554
clgo:orpha	39041

About: clgr:Omenn_syndrome