About: complement component 3 deficiency

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

Xref MGI.

Attributes	Values
type	Class
subClassOf	complement deficiency
label	complement component 3 deficiency
comment	Xref MGI.
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:8354
database_cross_reference	NCI:C9468 OMIM:613779 ORDO:280133 SNOMEDCT_US_2021_09_01:771443008 UMLS_CUI:C1332655
has_exact_synonym	C3 deficiency (en)
has_obo_namespace	disease_ontology
in_subset	DO_rare_slim NCIthesaurus
http://purl.obolib...g/obo/IAO_0000115	A complement deficiency that is characterized by deficiency of complement component 3 that increases susceptibility to infection and autoimmune diseases and has_material_basis_in autosomal recessive inheritance of mutation in the C3 gene on chromosome 19p13.3, has_symptom recurrent bacterial infections.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50955731

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