Disease #03449 (C9D (complement component 9 deficiency (C9D)), OMIM:613825)

Official abbreviation C9D
Name complement component 9 deficiency (C9D)
OMIM ID 613825
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene C9
Associated tissues -
Disease features -
Remarks -