|
retinitis pigmentosa caused by mutation in PDE6G
|
13315 |
|
|
Rickettsia helvetica caused disease or disorder
|
331 |
|
|
Mycobacterium marinum caused skin disease
|
43314 |
|
|
SCID, t cell-negative, b cell-negative, NK cell-positive
|
C563311 |
|
|
genetic transient congenital hypothyroidism
|
44331 |
|
|
hereditary transient congenital hypothyroidism
|
44331 |
|
|
adrenal hyperplasia, congenital, due to cytochrome P450 oxidoreductase deficiency
|
13310 |
|
|
dystrophy, hereditary corneal
|
D003317 |
|
|
granular dystrophy, corneal
|
D003317 |
|
|
stromal dystrophies, corneal
|
D003317 |
|
|
stromal dystrophy, corneal
|
D003317 |
|
|
MCFD2 combined deficiency of factor V and factor VIII
|
13331 |
|
