Disease #02459 (FHL2 (lymphohistiocytosis, hemophagocytic, familial, type 2 (FHL-2)), OMIM:603553)

Official abbreviation FHL2
Name lymphohistiocytosis, hemophagocytic, familial, type 2 (FHL-2)
OMIM ID 603553
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene PRF1
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

2 entries on 1 page. Showing entries 1 - 2.
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00174856 Patient van Kuilenburg, submitted - M no Netherlands - 00y02m - - - ?, FHL2 , fever, hepatosplenomegaly, persistent lactate acidosis, severely disturbed liver enzymes and ultimately multi-organ failure PRF1, SLC28A1 PRF1, SLC28A1 4 1 André van Kuilenburg
00306230 137 - - M - China - - - - - FHL2 - PRF1 PRF1 2 1 Sha Hong
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