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familial hemophagocytic lymphohistiocytosis 4 | RareConnect | RareConnect.io

/hereditary hemophagocytic lymphohistiocytosis

/familial hemophagocytic lymphohistiocytosis 4

familial hemophagocytic lymphohistiocytosis 4

Rare Disease

MONDO:0011336

Also Known As

FHL4HLH4HPLH4STX11 genetic hemophagocytic lymphohistiocytosisfamilial hemophagocytic lymphohistiocytosis 4familial hemophagocytic lymphohistiocytosis type 4genetic hemophagocytic lymphohistiocytosis caused by mutation in STX11hemophagocytic lymphohistiocytosis, familial, type 4Hlh4Hplh4hemophagocytic lymphohistiocytosis, familial, 4

Definition

Any genetic hemophagocytic lymphohistiocytosis in which the cause of the disease is a mutation in the STX11 gene.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:603552 ↗

GARD

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familial hemophagocytic lymphohistiocytosis 2

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Hermansky-Pudlak syndrome 2

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familial hemophagocytic lymphohistiocytosis 3

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