|
TULP1 Leber congenital amaurosis
|
13457 |
|
|
night blindness, congenital stationary, type 1D
|
13450 |
|
|
night blindness, congenital stationary, type 1D; CSNB1D
|
http://purl.obolibrary.org/obo/MONDO_0013450 |
|
|
adenofibroma of corpus uteri
|
3458 |
|
|
fibrosing alveolitis, cryptogenic
|
8345 |
|
|
intraventricular septal defect
|
D006345 |
|
|
intraventricular septal defects
|
D006345 |
|
|
dihydrofolate reductase deficiency
|
13456 |
|
|
histidine ammonia-lyase deficiency
|
9345 |
|
|
navajo immune deficient poikiloderma
|
C538345 |
|
|
familial frontonasal dermoid cysts
|
C563455 |
|
|
Oropouche virus disease or disorder
|
345 |
|
|
Schistosoma mansoni disease or disorder
|
44345 |
|
|
disease or disorder of cochlea
|
3452 |
|
