|
lectin complement activation pathway, defect in, 2
|
13423 |
|
|
Meier-Gorlin syndrome caused by mutation in ORC4
|
13428 |
|
|
retinitis pigmentosa caused by mutation in PDE6B
|
13429 |
|
|
retinitis pigmentosa caused by mutation in RPE65
|
13425 |
|
|
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 |
|
|
chromosome 3, monosomy 3p25
|
13424 |
|
|
C8 Alpha-gamma deficiency
|
13422 |
|
|
CX3CR1 age-related macular degeneration
|
13420 |
|
|
age related macular degeneration 12
|
13420 |
|
|
age related macular degeneration type 12
|
13420 |
|
