Disease #03141 (C6D (complement component 6 deficiency (C6D)), OMIM:612446)

Official abbreviation C6D
Name complement component 6 deficiency (C6D)
OMIM ID 612446
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene C6
Associated tissues -
Disease features -
Remarks -