Genomics England
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Genes and Entities
SERPIND1
serpin family D member 1
OMIM:
142360
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Mode of inheritance
Details
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Thrombophilia with a likely monogenic cause
R-numbers:
R97
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Thrombophilia due to heparin cofactor II deficiency, OMIM:612356