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 |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
UNC13D |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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