Search Ontology:
Human Disease

complement component 9 deficiency

Term ID
DOID:0060303
Synonyms
Definition
A complement deficiency that is characterized by recurrent bacterial infections, has_material_basis_in mutation in the C9 gene. https://www.omim.org/entry/613825
References
Ontology
Human Disease   ( DOID:0060303 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Human Gene Zebrafish Ortholog OMIM Term Disease OMIM Phenotype ID
C9C9 deficiencycomplement component 9 deficiency613825
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Zebrafish Models
No data available
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