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- Omenn_syndrome abstract "Omenn syndrome is an autosomal recessive severe combined immunodeficiency associated with mutations in the recombination activating genes (RAG1 and RAG2), affecting circulating levels of both B-cells and T-cells.".
- Omenn_syndrome diseasesdb "32676".
- Omenn_syndrome emedicineSubject "ped".
- Omenn_syndrome emedicineTopic "1640".
- Omenn_syndrome icd10 "D81.2 (ILDS D81.210)".
- Omenn_syndrome omim "603554".
- Omenn_syndrome thumbnail Omenn_syndrome.png?width=300.
- Omenn_syndrome wikiPageID "2294715".
- Omenn_syndrome wikiPageRevisionID "541691832".
- Omenn_syndrome diseasesdb "32676".
- Omenn_syndrome emedicinesubj "ped".
- Omenn_syndrome emedicinetopic "1640".
- Omenn_syndrome hasPhotoCollection Omenn_syndrome.
- Omenn_syndrome icd "D81.2".
- Omenn_syndrome name "Omenn syndrome".
- Omenn_syndrome omim "603554".
- Omenn_syndrome wordnet_type synset-disease-noun-1.
- Omenn_syndrome subject Category:Autosomal_recessive_disorders.
- Omenn_syndrome subject Category:Combined_T_and_B–cell_immunodeficiencies.
- Omenn_syndrome subject Category:Hepatology.
- Omenn_syndrome subject Category:Noninfectious_immunodeficiency-related_cutaneous_conditions.
- Omenn_syndrome subject Category:Rare_diseases.
- Omenn_syndrome subject Category:Syndromes.
- Omenn_syndrome type Abstraction100002137.
- Omenn_syndrome type Attribute100024264.
- Omenn_syndrome type AutosomalRecessiveDisorders.
- Omenn_syndrome type Cognition100023271.
- Omenn_syndrome type Complex105870365.
- Omenn_syndrome type Concept105835747.
- Omenn_syndrome type Condition113920835.
- Omenn_syndrome type Content105809192.
- Omenn_syndrome type Disease114070360.
- Omenn_syndrome type Disorder114052403.
- Omenn_syndrome type Idea105833840.
- Omenn_syndrome type IllHealth114052046.
- Omenn_syndrome type Illness114061805.
- Omenn_syndrome type NoninfectiousImmunodeficiency-relatedCutaneousConditions.
- Omenn_syndrome type PathologicalState114051917.
- Omenn_syndrome type PhysicalCondition114034177.
- Omenn_syndrome type PsychologicalFeature100023100.
- Omenn_syndrome type State100024720.
- Omenn_syndrome type Syndrome105870790.
- Omenn_syndrome type Syndromes.
- Omenn_syndrome type Whole105869584.
- Omenn_syndrome type Disease.
- Omenn_syndrome type AilmentCondition.
- Omenn_syndrome type Situation.
- Omenn_syndrome comment "Omenn syndrome is an autosomal recessive severe combined immunodeficiency associated with mutations in the recombination activating genes (RAG1 and RAG2), affecting circulating levels of both B-cells and T-cells.".
- Omenn_syndrome label "Omenn syndrome".
- Omenn_syndrome label "Syndroom van Omenn".
- Omenn_syndrome label "Síndrome de Omenn".
- Omenn_syndrome label "Zespół Omenna".
- Omenn_syndrome sameAs Síndrome_de_Omenn.
- Omenn_syndrome sameAs Syndroom_van_Omenn.
- Omenn_syndrome sameAs Zespół_Omenna.
- Omenn_syndrome sameAs m.071l_y.
- Omenn_syndrome sameAs Q2214419.
- Omenn_syndrome sameAs Q2214419.
- Omenn_syndrome sameAs 863.
- Omenn_syndrome sameAs Omenn_syndrome.
- Omenn_syndrome wasDerivedFrom Omenn_syndrome?oldid=541691832.
- Omenn_syndrome depiction Omenn_syndrome.png.
- Omenn_syndrome isPrimaryTopicOf Omenn_syndrome.
- Omenn_syndrome name "Omenn syndrome".
