toIPA
Home
Blog
Category
Hemochromatosis type 3
hemochromatosis that has material basis in homozygous or compound heterozygous mutation in the TFR2 gene on chromosome 7q22
Pronunciation
/ˌhiməˌkroʊməˈtoʊsɪs taɪp 3/
Categories
genetic disease
iron overload
HFE hereditary haemochromatosis
rare disease