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#616004 - DYSFIBRINOGENEMIA, CONGENITAL
HYPODYSFIBRINOGENEMIA, CONGENITAL, INCLUDED
Cytogenetic locations: STQTL12, STQTL12, 1p36
Gene summaries Genetic tests Medical literature
#202400 - AFIBRINOGENEMIA, CONGENITAL
HYPOFIBRINOGENEMIA, CONGENITAL, INCLUDED
Cytogenetic locations: at, lod, max
*134820 - FIBRINOGEN, A ALPHA POLYPEPTIDE; FGA
Cytogenetic locations: 12070049
#105200 - AMYLOIDOSIS, HEREDITARY SYSTEMIC 2; AMYLD2
Cytogenetic locations: 1p36, -, 1p36, 618455
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