Search Ontology:
Human Disease

complement component 2 deficiency

Term ID
DOID:0060295
Synonyms
Definition
A complement deficiency that is characterized by recurrent bacterial infections, has_material_basis_in autosomal recessive inheritance of mutation in the C2 gene. https://rarediseases.info.nih.gov/diseases/1452/complement-component-2-deficiency
References
Ontology
Human Disease   ( DOID:0060295 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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