|
enterocyte intrinsic factor receptor, defect of
|
100156 |
|
|
congenital cataract microcornea with corneal opacity
|
10015 |
|
|
megaloblastic anemia, Norwegian type
|
100157 |
|
|
sclerocornea with Other ocular anomalies
|
10015 |
|
|
multicentric osteolyses, idiopathic
|
D010015 |
|
|
multicentric osteolysis, idiopathic
|
D010015 |
|
|
enterocyte cobalamin malabsorption
|
100156 |
|
|
diffuse cystic angiomatosis of bone
|
D010015 |
|
|
pernicious anemia, juvenile, due to selective intestinal malabsorption of vitamin b12, with proteinuria
|
100156 |
|
|
Imerslund-Grasbeck syndrome type 2
|
100157 |
|
|
idiopathic multicentric osteolyses
|
D010015 |
|
|
idiopathic multicentric osteolysis
|
D010015 |
|
|
sclerocornea with other ocular anomalies
|
10015 |
|
|
PXDN anterior segment dysgenesis
|
10015 |
|
|
corneal opacification with Other ocular anomalies
|
10015 |
|
