|
familial medullary thyroid carcinoma
|
DOID_0050547 |
|
|
thyroid gland medullary carcinoma
|
DOID_3973 |
|
|
acrodermatitis
|
DOID_2722 |
|
|
endpoint modifier
|
BAO_0002170 |
|
|
2-hydroxyglutaric aciduria
|
DOID_0050573 |
|
|
ln
|
BAO_0002171 |
|
|
cone-rod dystrophy
|
DOID_0050572 |
|
|
log
|
BAO_0002172 |
|
|
D-2-hydroxyglutaric aciduria
|
DOID_0050575 |
|
|
mean
|
BAO_0002173 |
|
|
L-2-hydroxyglutaric aciduria
|
DOID_0050574 |
|
|
choledocholithiasis
|
DOID_11755 |
|
|
common bile duct disease
|
DOID_4137 |
|
|
hypochromic anemia
|
DOID_11759 |
|
|
Klippel-Feil syndrome
|
DOID_10426 |
|
|
solid phase
|
BAO_0002163 |
|
|
cranioectodermal dysplasia
|
DOID_0050577 |
|
|
liquid phase
|
BAO_0002164 |
|
|
silencing RNA modification method
|
BAO_0002165 |
|
|
occult macular dystrophy
|
DOID_0050578 |
|
