|
helicoidal peripapillary chorioretinal degeneration
|
C566236 |
|
|
dilated, 1u cardiomyopathy
|
C566296 |
|
|
spastic, with congenital miosis ataxia
|
C566247 |
|
|
apolipoprotein C-III deficiency
|
C566270 |
|
|
deficiency or defect of apolipoprotein e
|
C566260 |
|
|
apolipoprotein e, deficiency or defect of
|
C566260 |
|
|
atrial septal defect with atrioventricular conduction defects
|
C566238 |
|
|
peripapillary chorioretinal degeneration, icelandic type
|
C566236 |
|
|
right ventricular dilated cardiomyopathy
|
C566255 |
|
|
bpes with duane retraction syndrome
|
C566222 |
|
|
hemorrhagic disorder due to an acquired coagulation factor defect
|
15662.0 |
|
|
rare bleeding disorder due to an acquired coagulation factor defect
|
http://purl.obolibrary.org/obo/MONDO_0015662 |
|
|
rare coagulopathy due to an acquired coagulation factor defect
|
http://purl.obolibrary.org/obo/MONDO_0015662 |
|
|
antibody deficiency due to defect in CD19
|
C566275 |
|
|
alpha-1 related emphysema
|
C566273 |
|
