has material basis in germline mutation in FTL hereditary disease hematologic disorder L-ferritin deficiency https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/l_ferritin_deficiency GARD:0017748 MEDGEN:816420 UMLS:C3810090 MONDO:0014274 LFTD L-ferritin deficiency Orphanet:440731 OMIM:615604 L-ferritin deficiency, dominant and recessive