About: immunodeficiency 50

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An Entity of Type : owl:Class, within Data Space : demo.openlinksw.com associated with source document(s)

Attributes	Values
type	Class
subClassOf	X-linked recessive disease combined immunodeficiency nodeID://b50945896
label	immunodeficiency 50
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0112001
database_cross_reference	OMIM:300988 ORDO:504530
has_exact_synonym	CID due to Moesin deficiency IMD50 MSN-related combined immunodeficiency X-linked Moesin-associated immunodeficiency combined immunodeficiency due to Moesin deficiency immunodeficiency 50 X linked recessive
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A combined immunodeficiency characterized by profound lymphopenia, hypogammaglobulinemia, poor immune response to vaccine antigens, fluctuating neutropenia and onset in early childhood of recurrent bacterial or varicella zoster virus infections that has_material_basis_in hemizygous mutation in MSN on chromosome Xq12.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50945897

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