|
post-traumatic stress disorders
|
D013313 |
|
|
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 |
|
|
Charcot-Marie-Tooth disease, demyelinating, type 1G
|
33135 |
|
|
Rickettsia helvetica disease or disorder
|
331 |
|
|
PMP2-related Charcot-Marie-Tooth disease type 1
|
33135 |
|
|
coronary heart disease, susceptibility to, 3
|
10331 |
|
|
coronary heart disease, susceptibility to, type 3
|
10331 |
|
