Disease #04407 (CFBD (deficiency, complement factor B? (CFBD)), OMIM:615561)

Official abbreviation CFBD
Name deficiency, complement factor B? (CFBD)
OMIM ID 615561
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene CFB
Associated tissues -
Disease features -
Remarks -