About: type I complement component 8 deficiency

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An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

NT MGI.

Attributes	Values
type	Class
subClassOf	complement deficiency
label	type I complement component 8 deficiency
comment	NT MGI.
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0060301
created_by	emitraka
creation_date	2015-02-09T15:32:25Z
database_cross_reference	ICD10CM:D84.1 OMIM:613790 ORDO:169150
has_obo_namespace	disease_ontology
in_subset	DO_rare_slim
http://purl.obolib...g/obo/IAO_0000115	A complement deficiency that is characterized by deficiency of the alpha subunit of complement protein 8, which causes increased susceptibility to recurrent bacterial infections, especially to Neisseria meningitidis, and has_material_basis_in autosomal recessive inheritance of mutation in the C8A gene, which produces the alpha subunit of complement component 8 important in forming membrane attack complexes.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50938614

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