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Disease Ontology Browser
hyperferritinemia-cataract syndrome (DOID:0111256)
Alliance: disease page
Synonyms: Bonneau-Beaumont syndrome; cataract-hyperferritinemia syndrome; hereditary hyperferritinemia with congenital cataracts; hereditary hyperferritinemia-cataract syndrome; HHCS; HRFTC; hyperferritinemia with or without cataract
Alt IDs: OMIM:600886, MESH:C538137, ORDO:163, UMLS_CUI:C1833213
Definition: A syndrome characterized by elevated circulating levels of ferritin without iron overload and early onset cataracts that has_material_basis_in heterozygous mutation in the iron responsive element in the 5-prime noncoding region of FTL on 19q13.33.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
09/27/2022
MGI 6.21
The Jackson Laboratory