familial hemophagocytic lymphohistiocytosis 2
hemophagocytic lymphohistiocytosis that has material basis in an autosomal recessive mutation of PRF1 on chromosome 10q22.1
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familial hemophagocytic lymphohistiocytosis 2
Summary
familial hemophagocytic lymphohistiocytosis 2 is a rare disease[1].
Key Facts
- familial hemophagocytic lymphohistiocytosis 2's instance of is recorded as rare disease[2].
- familial hemophagocytic lymphohistiocytosis 2's instance of is recorded as class of disease[3].
- familial hemophagocytic lymphohistiocytosis 2 is a type of familial hemophagocytic lymphohistiocytosis[4].
- familial hemophagocytic lymphohistiocytosis 2 is a type of genetic disease[5].
- familial hemophagocytic lymphohistiocytosis 2 is a type of autosomal recessive disease[6].
- familial hemophagocytic lymphohistiocytosis 2 is a type of hemophagocytic lymphohistiocytosis[7].
- familial hemophagocytic lymphohistiocytosis 2's genetic association is recorded as PRF1[8].
- familial hemophagocytic lymphohistiocytosis 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110922[9].
- familial hemophagocytic lymphohistiocytosis 2's exact match is recorded as http://identifiers.org/doid/DOID:0110922[10].
- familial hemophagocytic lymphohistiocytosis 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_540[11].
- familial hemophagocytic lymphohistiocytosis 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].