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

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000326908 premature birth reduced hemoglobin, thrombocytopenia purpura ascites, splenomegaly hemophagocytic syndrome FHL3 Isolated (sporadic) 00y00m19d00h 00y02m09d00h 00y00m19d00h - - Yanhong Li 00436783
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