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Vogt–Koyanagi–Harada syndromeNorman–Roberts syndromemyelofibrosisAutosomal dominant retinal vasculopathy with cerebral leukodystrophysea-blue histiocyte syndromeacidophil adenomaAutoimmune polyendocrine syndrome type 3chromosome 5q deletion syndromeAplasia cutis congenita-intestinal lymphangiectasia syndromeAagenaes syndromehereditary neutrophiliaLymphedema–distichiasis syndromeMikulicz diseaseExtracutaneous mastocytomaEmberger syndromebreast diffuse large B-cell lymphomahypersensitivity pneumonitis, familialWolfram-like syndromeautosomal dominant aplasia and myelodysplasiapulmonary fibrosis and/or bone marrow failure, Telomere-related, 1pancytopenia-developmental delay syndromepulmonary fibrosis and/or bone marrow failure, Telomere-related, 4pulmonary fibrosis and/or bone marrow failure, Telomere-related, 314q32 duplication syndromehereditary thrombocytopenia with early-onset myelofibrosisaggressive primary cutaneous B-cell lymphomaindolent primary cutaneous B-cell lymphomaprimary lymphoma of the conjunctivafamilial chilblain lupussubcutaneous panniculitis-like T-cell lymphomapanniculitis and localized lipodystrophyMicrocephaly lymphoedema chorioretinal dysplasiaSneddon syndromeReynolds syndromeSatoyoshi syndromecongenital pulmonary lymphangiectasia
P279
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P279
description
Rare genetic immune system disease
@en
name
rare genetic immune disease
@en
type
label
rare genetic immune disease
@en
altLabel
rare genetic immune system disease
@en
prefLabel
rare genetic immune disease
@en
P1550
P2888
P5270
MONDO:0015984