|
type II complement component 8 deficiency
|
13421 |
|
|
type I complement component 8 deficiency
|
13422 |
|
|
type i complement component 8 deficiency
|
http://purl.obolibrary.org/obo/MONDO_0013422 |
|
|
C8B classic complement early component deficiency
|
13421 |
|
|
C8A classic complement early component deficiency
|
13422 |
|
|
lectin complement activation pathway, defect in, 2
|
13423 |
|
|
macular degeneration, age-related, 12
|
13420 |
|
|
macular degeneration, age-related, 12; ARMD12
|
http://purl.obolibrary.org/obo/MONDO_0013420 |
|
|
macular Degeneration, age-related, type 12
|
13420 |
|
|
chromosome 3pter-p25 deletion syndrome
|
13424 |
|
|
C8 Alpha-gamma deficiency
|
13422 |
|
|
CX3CR1 age-related macular degeneration
|
13420 |
|
|
nervous system diseases, parasympathetic
|
D001342 |
|
|
classic complement early component deficiency caused by mutation in C8A
|
13422 |
|
|
classic complement early component deficiency caused by mutation in C8B
|
13421 |
|
