Disease #01717 (C2D (complement component 2 deficiency (C2D)), OMIM:217000)

Official abbreviation C2D
Name complement component 2 deficiency (C2D)
OMIM ID 217000
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene C2
Associated tissues -
Disease features -
Remarks -