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familial hemophagocytic lymphohistiocytosis 3 | RareConnect | RareConnect.io

/hereditary hemophagocytic lymphohistiocytosis

/familial hemophagocytic lymphohistiocytosis 3

familial hemophagocytic lymphohistiocytosis 3

Rare Disease

MONDO:0012146

Also Known As

FHL3HLH3HPLH3UNC13D genetic hemophagocytic lymphohistiocytosisfamilial hemophagocytic lymphohistiocytosis type 3genetic hemophagocytic lymphohistiocytosis caused by mutation in UNC13Dhemophagocytic lymphohistiocytosis, familial, type 3Hlh3Hplh3hemophagocytic lymphohistiocytosis, familial, 3

Definition

Any genetic hemophagocytic lymphohistiocytosis in which the cause of the disease is a mutation in the UNC13D 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:608898 ↗

GARD

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