has characteristic has characteristic has material basis in germline mutation in FTL hereditary disease eye disorder hereditary hyperferritinemia with congenital cataracts https://github.com/monarch-initiative/mondo/issues/4069 https://www.malacards.org/card/hyperferritinemia_with_or_without_cataract MONDO:0010952 UMLS:C1833213 SCTID:702398007 cataract-hyperferritinemia syndrome Hereditary hyperferritinemia with congenital cataracts is characterized by the association of early onset (although generally absent at birth) cataract with persistently raised plasma ferritin concentrations in the absence of iron overload. Hyperferritinemia Cataract Syndrome MEDGEN:318812 OMIM:600886 hyperferritinemia cataract syndrome GARD:0002806 MESH:C538137 ICD9:289.89 HHCS Orphanet:163 hereditary hyperferritinemia cataract syndrome DOID:0111256 hereditary hyperferritinemia-cataract syndrome ICD9:366.44 NORD:1264 HRFTC congenital