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Showing below up to 50 results in range #8,101 to #8,150.
- Deficiency of coagulation factor due to other cause of vitamin K deficiency (Q104709)
- Congenital mesoblastic nephroma (Q104708)
- Factor X deficiency associated with systemic amyloidosis (Q104707)
- Deficiency of coagulation factor due to vitamin K malabsorption in obstructive biliary disease (Q104706)
- Necrosis of nasal septum (Q104705)
- Deficiency of coagulation factor due to vitamin K malabsorption in intestinal disease (Q104704)
- Proliferative diabetic retinopathy without macular oedema due to drug or chemical induced diabetes mellitus (Q104703)
- Galloway Mowat syndrome (Q104702)
- Pierson syndrome (Q104701)
- Acquired prothrombin complex deficiency (Q104700)
- Acquired von Willebrand disease (Q104699)
- Deficiency of coagulation factor due to nutritional vitamin K deficiency (Q104698)
- Cellulitis of nasal septum (Q104697)
- 9340/0 (Q104696)
- 9310/0 (Q104695)
- Mycobacterial epidural abscess (Q104694)
- Ulceration of nasal septum (Q104693)
- 9321/0 (Q104692)
- 9281/0 (Q104691)
- 9300/0 (Q104690)
- 9301/0 (Q104689)
- 9310/3 (Q104688)
- 9341/3 (Q104687)
- 9342/3 (Q104686)
- 9302/3 (Q104685)
- 9330/3 (Q104684)
- 9322/0 (Q104683)
- 9290/3 (Q104682)
- 9311/0 (Q104681)
- 9290/0 (Q104680)
- 9282/0 (Q104679)
- 9330/0 (Q104678)
- 9320/0 (Q104677)
- 9302/0 (Q104676)
- 9312/0 (Q104675)
- 9280/0 (Q104674)
- 9271/0 (Q104673)
- 9275/0 (Q104672)
- 9274/0 (Q104671)
- 9270/0 (Q104670)
- 9273/0 (Q104669)
- 9272/0 (Q104668)
- Charcot-Marie-Tooth disease type 4G (Q104667)
- 9270/3 (Q104666)
- Charcot-Marie-Tooth disease type 4B2 (Q104665)
- Charcot-Marie-Tooth disease 1X, x-linked Charcot-Marie-Tooth disease 1 due to mutations in gap junction protein beta 1 (Q104664)
- 9270/1 (Q104663)
- Charcot-Marie-Tooth disease type 4B1 (Q104662)
- Postpartum fibrinolysis with haemorrhage (Q104661)
- Charcot-Marie-Tooth disease type 4J (Q104660)
