About: immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia

Not logged in : Login

(Sponging disallowed)

Facets (new session)
Description
Metadata
Settings
- Rule:
- Inverse Functional Properties:
- "Same As":

About: immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia Goto Sponge NotDistinct Permalink

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

Attributes	Values
type	Class
subClassOf	autosomal recessive disease combined immunodeficiency nodeID://b50946005
label	immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0112062
database_cross_reference	OMIM:618987
has_exact_synonym	IMD73C
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A combined immunodeficiency characterized by onset of recurrent infection in early childhood, impaired neutrophil chemotaxis, decreased B cells, hypogammaglobulinemia, and other variable features that has_material_basis_in homozygous or compound heterozygous mutation in RAC2 on chromosome 22q12.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50946006

Faceted Search & Find service v1.17_git150 as of Jan 20 2025

Alternative Linked Data Documents: iSPARQL | ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 08.03.3332 as of Jan 29 2025, on Linux (x86_64-generic-linux-glibc25), Single-Server Edition (378 GB total memory, 38 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2025 OpenLink Software