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Chondrodysplasia Punctata with Coagulation Factor Deficiency (DOID:9002967)
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Parent Terms Term With Siblings Child Terms
Astley-Kendall Syndrome 
autosomal dominant chondrodysplasia punctata +  
Chondrodysplasia Punctata with Coagulation Factor Deficiency 
combined deficiency of vitamin K-dependent clotting factors 2  
congenital afibrinogenemia +   
Congenital Plasminogen Deficiency 
Dysfibrinogenemia Causing Recurrent Thrombosis 
factor V deficiency +   
factor VII deficiency  
factor VIII deficiency +   
factor X deficiency  
factor XI deficiency  
factor XII deficiency  
factor XIII deficiency +   
Flood Factor Deficiency 
hemophilia B  
Pacman Dysplasia 
prothrombin deficiency +   
Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency  
rhizomelic chondrodysplasia punctata +   
Tatsumi Factor Deficiency 
thrombophilia due to activated protein C resistance  
von Willebrand's disease +   
X-linked chondrodysplasia punctata 1  
X-linked chondrodysplasia punctata 2  

Primary IDs: MESH:C564742 ;   RDO:0013603

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