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Disease association ontology term - MONDO:0004805 - leukocyte disorder

Term summary

ID
MONDO:0004805
Name
leukocyte disorder
Ontology or CV name
Disease association
Definition
A disease involving leukocytes.

Parents

Annotation

Disease association

MONDO:0030519 - agammaglobulinemia 9, autosomal recessive

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MONDO:0008963 - Chediak-Higashi syndrome

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MONDO:0014118 - congenital neutropenia-myelofibrosis-nephromegaly syndrome

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MONDO:0010600 - granulomatous disease, chronic, X-linked

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MONDO:0011997 - Hermansky-Pudlak syndrome 2

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MONDO:0011971 - hyper-IgM syndrome type 5

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MONDO:0958013 - immunodeficiency, common variable, 15

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MONDO:0009953 - leukocyte adhesion deficiency type II

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MONDO:0957809 - neutropenia, severe congenital, 10, autosomal recessive

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MONDO:0958017 - neutropenia, severe congenital, 11, autosomal dominant

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MONDO:0980936 - neutropenia, severe congenital, 12, autosomal recessive

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MONDO:0032899 - neutropenia, severe congenital, 8, autosomal dominant

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MONDO:0030726 - neutropenia, severe congenital, 9, autosomal dominant

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MONDO:0008214 - Pelger-Huet anomaly

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MONDO:0009693 - plasma cell myeloma

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MONDO:0011405 - poikiloderma with neutropenia

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MONDO:0012559 - primary immunodeficiency syndrome due to p14 deficiency

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MONDO:0018542 - severe congenital neutropenia

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MONDO:0044208 - specific granule deficiency 2

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MONDO:0001892 - spinal cord lymphoma

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MONDO:0020332 - systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease

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MONDO:0010294 - X-linked severe congenital neutropenia

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