|
complement component 8 deficiency, type I; C8D1
|
http://purl.obolibrary.org/obo/MONDO_0013422 |
|
|
complement component 8 deficiency, type II
|
13421 |
|
|
complement component 8 deficiency, type II; C8D2
|
http://purl.obolibrary.org/obo/MONDO_0013421 |
|
|
complement component 8B deficiency
|
13421 |
|
|
chromosome 3pter-p25 deletion syndrome
|
13424 |
|
|
Meier-GORLIN syndrome 2; MGORS2
|
http://purl.obolibrary.org/obo/MONDO_0013428 |
|
|
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 |
|
|
Human complement C8-beta deficiency
|
13421 |
|
|
Meier-Gorlin syndrome caused by mutation in ORC4
|
13428 |
|
|
retinitis pigmentosa caused by mutation in PDE6B
|
13429 |
|
