Skip Header

You are using a version of browser that may not display all the features of this website. Please consider upgrading your browser.

Definition

An autosomal dominant disease characterized by elevated level of ferritin in serum and tissues, and early-onset bilateral cataract. Cataracts may be subclinical in some patients.

Acronym

HRFTC

Synonyms

HHCS
Hyperferritinemia, hereditary, with congenital cataracts
Hyperferritinemia-cataract syndrome

Keywords

Cataract