Disease #02801 (FHL3 (lymphohistiocytosis, hemophagocytic, familial, type 3 (FHL-3)), OMIM:608898)

Official abbreviation FHL3
Name lymphohistiocytosis, hemophagocytic, familial, type 3 (FHL-3)
OMIM ID 608898
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene UNC13D
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00436783 - - 1-generation family, 1 affected, unaffected heterozygous carrier parents F no China Asia-E - - - - FHL3 premature birth reduced hemoglobin, thrombocytopenia purpura ascites, splenomegaly UNC13D UNC13D 2 1 Yanhong Li
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