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...in between 0.3 and 0.8% of Caucasians.<ref>{{cite journal|title=Hereditary hemochromatosis|journal=Rev Med Interne|year=2000 |volume=21 |issue=11 |pages=961–71 |doi

|-HHC or GHC(Haemochromatotis. Also Hemochromatosis) | Hereditary Motor and Sensory Polyneuropathy Type III (see [[Dejerine Sottas syndrome]]

...f>{{cite journal |author=Centola M, Aksentijevich I, Kastner DL |title=The hereditary periodic fever syndromes: molecular analysis of a new family of inflammator *[[Marie–Unna hereditary hypotrichosis]] (Marie–Unna hypotrichosis)

* [[Neonatal hemochromatosis]] * [[Neuropathy hereditary with liability to pressure palsies]]

* [[Heart hypertrophy, hereditary]] '''Hereditary a-Hereditary m'''

| Anemia, hereditary sideroblastic <br><small>''see'' [[X-linked sideroblastic anemia]] </small> | Arthro-ophthalmopathy, hereditary progressive <br><small>''see'' [[Stickler syndrome#COL2A1]] </small> || ||

...K, Schatzman RC, Feder JN |title=A 1.1-Mb transcript map of the hereditary hemochromatosis locus |year=1997 |month=May |volume=7 |issue=5 |pages=441–56 |pmid= 91499 ...rgan K, Tenenhouse HS, Juppner H |title=SLC34A3 mutations in patients with hereditary hypophosphatemic rickets with hypercalciuria predict a key role for the sod