Connective Tissue

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