Hemochromatosis type 1

Hemochromatosis type 1 is a hepatic/metabolic genetic disease caused by autosomal recessive variants in BMP2, HFE. It is not placed in the rankable burden order: only 2 of five axes are scored (cut: three of five), so the remaining 3 stay open [O], not guessed. Mechanism, scored axes, and treatment follow below.

Hemochromatosis type 1 is inherited as autosomal recessive and acts by loss-of-function (biallelic; recessive) ([H]). Of the five burden axes, 2 are scored (P, S) and 3 are open [O] (O, M, D); because fewer than three are scored the disease is reported as “not placed — insufficient axis coverage” (rank null), not ranked on partial data.

Gene, inheritance, and molecular mechanism

Hemochromatosis type 1 is inherited as Autosomal recessive inheritance [L] and is classified mechanistically as loss-of-function (biallelic; recessive) [H]. HFE regulates hepcidin, the master iron-regulatory hormone. Loss of HFE function lowers hepcidin, so intestinal iron absorption is inappropriately high and iron deposits in parenchymal organs.

Inheritance source: medgen:esummary:ModeOfInheritance:2026-06-17. Mechanism source: inference:recessive=>loss_of_function; basis=medgen_inheritance(recessive); corrob=clingen_AR(HI30):HFE. These are observed, cited inputs; the classification is the reproducible analysis layer (C-D1).

In-scope clinical involvement

Progressive iron overload in mid-adult life causes hepatic cirrhosis, diabetes mellitus, cardiomyopathy, arthropathy, and skin pigmentation.

Organ systems [L] from HPO phenotype.hpoa v2026-06-06 (OMIM 235200,613609); P-aspect terms rolled up to HP:0000118 organ-system categories via hp.obo.

Burden axes and why this disease is not placed

For transparency the partial composite over the 2 scored axis/axes is raw_burden = 0.6250, but it is not used to rank the disease (below the ≥ 3-axis cut). The open axes (onset, mortality, disability) are graded [O] with a named obstacle, never imputed.

The natural-history registry passes lift onset (Orphanet, R6) and disability (GBD 2013 disability weights, R7) to registry [L] where an entity-anchored mapping exists, lift severity (HPO Severity-modifier subtree, R8) where the dominant sequela is annotated, and lift progression (curated PMC open-access literature with a frozen-R3-derived tier, R9) where a cited disease-level magnitude for the dominant untreated sequela exists. For some diseases the added disability axis was enough to cross the ≥ 3-axis cut and enter the placed residual order; for this one it was not — and its dominant sequela carries no open HPO severity annotation, so no registry severity tier is available (the open HPO severity annotations elsewhere are feature-level; the OMIM clinical synopsis, the disease-level alternative, is API-key-gated and the key is unobtainable for an individual researcher). Scoring three or more axes at registry grade (via published functional & survival literature) would let this disease enter the rankable residual order; until then it is reported here, never imputed.

Established treatment

The established disease-directed approach is therapeutic phlebotomy (iron chelation where phlebotomy is contraindicated). Mechanistically: phlebotomy depletes excess body iron stores [L]. Its effect on natural history is classified disease-modifying (substantial) (efficacy offset e = 0.5500, residual factor R_treat = 0.4500); this offset would apply to the burden score once the disease is placed.

Evidence tier: accession-dated to the GeneReviews NBK1440 Management section [L] (initial posting April 3, 2000; last revision April 11, 2024; retrieved 2026-06-18; corroborating term(s): “therapeutic, phlebotomy, iron, chelation”).