Disease #04471 (Dysfibrinogenemia, congenital, OMIM:616004)

Official abbreviation -
Name Dysfibrinogenemia, congenital
OMIM ID 616004
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 3 genes FGA, FGB, FGG
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Individuals

1 entry on 1 page. Showing entry 1.
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00380776 ? PubMed: Nair 2018 - ? - Lebanon - - 0 - - Dysfibrinogenemia, congenital Thromboembolic cerebral accident; short extremities; seizures (Immune/hematology) - FGA 1 1 LOVD
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