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- NP627377.RADzc_YtcthSgjb-zQk7EXHlPgVR4IU8_cH881FJa0tRY130_assertion type Assertion NP627377.RADzc_YtcthSgjb-zQk7EXHlPgVR4IU8_cH881FJa0tRY130_head.
- NP627377.RADzc_YtcthSgjb-zQk7EXHlPgVR4IU8_cH881FJa0tRY130_assertion description "[Then, the type of liver siderosis (parenchymal, mesenchymal or mixed) and its distribution throughout the lobule and the liver are useful means for suggesting its etiology: HLA-linked hemochromatosis gene (HFE) hemochromatosis or other rare genetic hemochromatosis, nonhemochromatotic genetic iron overload (ferroportin disease, aceruloplasminemia), or iron overload secondary to excessive iron supply, inflammatory syndrome, noncirrhotic chronic liver diseases including dysmetabolic iron overload syndrome, cirrhosis, and blood disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP627377.RADzc_YtcthSgjb-zQk7EXHlPgVR4IU8_cH881FJa0tRY130_provenance.
- NP627377.RADzc_YtcthSgjb-zQk7EXHlPgVR4IU8_cH881FJa0tRY130_assertion evidence source_evidence_literature NP627377.RADzc_YtcthSgjb-zQk7EXHlPgVR4IU8_cH881FJa0tRY130_provenance.
- NP627377.RADzc_YtcthSgjb-zQk7EXHlPgVR4IU8_cH881FJa0tRY130_assertion SIO_000772 17729397 NP627377.RADzc_YtcthSgjb-zQk7EXHlPgVR4IU8_cH881FJa0tRY130_provenance.
- NP627377.RADzc_YtcthSgjb-zQk7EXHlPgVR4IU8_cH881FJa0tRY130_assertion wasDerivedFrom befree-2016 NP627377.RADzc_YtcthSgjb-zQk7EXHlPgVR4IU8_cH881FJa0tRY130_provenance.
- NP627377.RADzc_YtcthSgjb-zQk7EXHlPgVR4IU8_cH881FJa0tRY130_assertion wasGeneratedBy ECO_0000203 NP627377.RADzc_YtcthSgjb-zQk7EXHlPgVR4IU8_cH881FJa0tRY130_provenance.