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Date: Tue Jan 28 2025
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thrombophilia due to HRG deficiency
DOID:0111903
Summary
Associated Genes
Associated Alleles
Associated Models
Disease
thrombophilia due to HRG deficiency
Definition
A thrombophilia characterized by decreased histidine-rich glycoprotein (HRG) plasma levels and a tendency to develop thrombosis that has_material_basis_in heterozygous mutation in HRG on chromosome 3q27.3.
[1]
[2]
Synonyms
hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
hereditary thrombophilia due to congenital HRG deficiency
Show All 3
Cross References
MIM:613116
ORDO:217467
Show All 3
Parent Terms
autosomal dominant disease
thrombophilia
Child Terms
None
Sources of Associations
RGD
MGI
ZFIN
FB
WB
SGD
Associated Genes
Associated Alleles
Associated Models
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