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Query OMIM entry list
169200
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PECHET FACTOR DEFICIENCY
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Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Coagulation Disorders
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Genetic Diseases, Inborn
Chromosome Disorders
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Database Center for Life Science
