|
corneal opacification and other ocular anomalies
|
10015 |
|
|
multicentric osteolyses, idiopathic
|
D010015 |
|
|
multicentric osteolysis, idiopathic
|
D010015 |
|
|
anterior segment dysgenesis 7
|
10015 |
|
|
anterior segment dysgenesis 7; ASGD7
|
http://purl.obolibrary.org/obo/MONDO_0010015 |
|
|
anterior segment dysgenesis caused by mutation in PXDN
|
10015 |
|
|
enterocyte intrinsic factor receptor, defect of
|
100156 |
|
|
congenital cataract microcornea with corneal opacity
|
10015 |
|
|
idiopathic multicentric osteolyses
|
D010015 |
|
|
idiopathic multicentric osteolysis
|
D010015 |
|
|
sclerocornea with other ocular anomalies
|
10015 |
|
|
Imerslund-Grasbeck syndrome type 1
|
100156 |
|
|
PXDN anterior segment dysgenesis
|
10015 |
|
|
megaloblastic Anemia type 1
|
100156 |
|
