| Disease |
Protein |
BMRB entry |
| Agranulocytosis |
Granulocyte colony-stimulating factor |
18291 |
| Arterial Calcification |
Calcium bound human S100A11 |
18425 |
| Atypical hemolytic uremic syndrome |
CCP modules 10-12 or factor H |
18599
18604 |
| Benign cephalic histiocytosis |
Cytosolic tails of axb2 integrin |
18542 |
| Cataracts |
P23T mutant of human gamma-D crystallin |
16173 |
|
Tudor domain containing 7 |
17835 |
| Osteogenesis Imperfecta |
Type-1 892 protein |
17470 |
| Hemophilia B |
Human fibrillin-1 |
17334 |
| Hughes syndrome |
Beta 2 glycoprotein |
16639 |
| Hypertension |
NK1 Autoinhibitory Domain |
18398 |
| Lupus erythematosus |
C-type lectin domain family 4 member D |
18415 |
| Marfan syndrome |
Human fibrillin-1 |
17334 |
| Neutropenia |
Granulocyte colony-stimulating factor |
18291 |
