|
Human complement C8-beta deficiency
|
13421 |
|
|
autosomal dominant 38 deafness
|
C563421 |
|
|
autosomal dominant 14 deafness
|
C563421 |
|
|
autosomal dominant 6 deafness
|
C563421 |
|
|
type II complement component 8 deficiency
|
13421 |
|
|
complement component 8 deficiency type 2
|
13421 |
|
|
complement component 8 deficiency type II
|
13421 |
|
|
complement component 8 deficiency, type 2
|
13421 |
|
|
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 |
|
