familial hemophagocytic lymphohistiocytosis 5
hemophagocytic lymphohistiocytosis that has material basis in a mutation of STXBP2 on chromosome 19p13.2
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familial hemophagocytic lymphohistiocytosis 5
Summary
familial hemophagocytic lymphohistiocytosis 5 is a rare disease[1].
Key Facts
- familial hemophagocytic lymphohistiocytosis 5's instance of is recorded as rare disease[2].
- familial hemophagocytic lymphohistiocytosis 5's instance of is recorded as class of disease[3].
- familial hemophagocytic lymphohistiocytosis 5 is a type of familial hemophagocytic lymphohistiocytosis[4].
- familial hemophagocytic lymphohistiocytosis 5 is a type of genetic disease[5].
- familial hemophagocytic lymphohistiocytosis 5 is a type of monogenic disease[6].
- familial hemophagocytic lymphohistiocytosis 5 is a type of hemophagocytic lymphohistiocytosis[7].
- familial hemophagocytic lymphohistiocytosis 5's genetic association is recorded as STXBP2[8].
- familial hemophagocytic lymphohistiocytosis 5's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110925[9].
- familial hemophagocytic lymphohistiocytosis 5's exact match is recorded as http://identifiers.org/doid/DOID:0110925[10].
- familial hemophagocytic lymphohistiocytosis 5's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_540[11].
- familial hemophagocytic lymphohistiocytosis 5's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].