WormMine

WS297

Intermine data mining platform for C. elegans and related nematodes

Disease Ontology : DOID:0111985 immunodeficiency 32B Disease Ontology

Namespace  disease_ontology Obsolete  false
Description  A monocyte, dendritic cell, and NK cell deficiency characterized by defects in monocyte, dendritic cell, and natural killer (NK) cell development or function resulting recurrent infections particularly viral nfections that has_material_basis_in homozygous or compound heterozygous mutation in the IRF8 gene on chromosome 16q24.1.

1 Ontology

Name
Disease Ontology

11 Parents

Identifier Name Description
DOID:7 disease of anatomical entity A disease that manifests in a defined anatomical structure.
DOID:4 disease A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism.
DOID:2914 immune system disease A disease of anatomical entity that is located_in the immune system.
DOID:612 primary immunodeficiency disease An immune system disease that results when one or more essential parts of the immune system is missing or not working properly at birth due to a genetic mutation.
DOID:0050177 monogenic disease A genetic disease that is the result of one or more abnormal alleles and may be dominant, semi-dominant, or recessive.
DOID:630 genetic disease A disease that has_material_basis_in genetic variations in the human genome.
DOID:0050739 autosomal genetic disease A monogenic disease that has_material_basis_in a mutation in a single gene on one of the non-sex chromosomes.
DOID:0050737 autosomal recessive disease An autosomal genetic disease that is characterized by the presence of two mutated copies of the gene, both of which must be present in order for the disease or trait to develop.
DOID:0111962 combined immunodeficiency A primary immunodeficiency disease that involves multiple components of the immune system.
DOID:0111966 monocyte, dendritic cell, and NK cell deficiency A combined immunodeficiency characterized by impaired function or reduced numbers of monocytes, dendritic cells, and natural killer (NK) cells.
DOID:0111985 immunodeficiency 32B A monocyte, dendritic cell, and NK cell deficiency characterized by defects in monocyte, dendritic cell, and natural killer (NK) cell development or function resulting recurrent infections particularly viral nfections that has_material_basis_in homozygous or compound heterozygous mutation in the IRF8 gene on chromosome 16q24.1.

10 Relations

Relationship
Parent Term . Identifier

Child Term . Identifier
is_a DOID:0111966 DOID:0111985
is_a DOID:0050737 DOID:0111985
is_a DOID:7 DOID:0111985
is_a DOID:0050739 DOID:0111985
is_a DOID:4 DOID:0111985
is_a DOID:0111962 DOID:0111985
is_a DOID:630 DOID:0111985
is_a DOID:2914 DOID:0111985
is_a DOID:612 DOID:0111985
is_a DOID:0050177 DOID:0111985

3 Synonyms

Name Type
autosomal recessive IRF8 deficiency synonym
IMD32B synonym
immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive synonym