Cystic fibrosis

Cystic fibrosis is a respiratory/exocrine genetic disease caused by autosomal recessive variants in CFTR, FCGR2A, TGFB1, acting through loss of function (a folding/trafficking defect for p.Phe508del). Within this volume's rankable burden cohort it sits at residual rank 17 of 23, where established therapy is substantially disease-modifying. That order is a provisional [H]-grade prioritisation device, not a registry-locked ranking.

Cystic fibrosis is inherited as autosomal recessive and acts by loss-of-function (incl. trafficking/folding defect for p.Phe508del) ([L]). Its pre-treatment burden proxy is 0.6833 and, after the established therapy's efficacy offset e = 0.5500 is applied, its residual burden score is 0.3075 ([H]), placing it at residual rank 17 of 23.

Gene, inheritance, and molecular mechanism

Cystic fibrosis is inherited as Autosomal recessive inheritance [L] and is classified mechanistically as loss-of-function (incl. trafficking/folding defect for p.Phe508del) [L]. CFTR encodes an epithelial chloride and bicarbonate channel. Loss of function -- for the common p.Phe508del allele, a protein folding and trafficking defect -- dehydrates secretions across many epithelia.

Inheritance source: medgen:esummary:ModeOfInheritance:2026-06-17. Mechanism source: curated_rule:cftr_lof; established molecular genetics; OMIM(row) molecular section; OMIM:219700. These are observed, cited inputs; the inheritance and mechanism classification is the reproducible analysis layer (C-D1).

In-scope clinical involvement

The disease affects the respiratory tract, exocrine pancreas, intestine, hepatobiliary system, and sweat glands, with bronchiectasis, recurrent sinusitis, pancreatic insufficiency, and a diagnostically elevated sweat chloride.

Organ systems [L] from HPO phenotype.hpoa v2026-06-06 (OMIM 219700,602421); P-aspect terms rolled up to HP:0000118 organ-system categories via hp.obo.

Reproducible burden position

Of the five axes, 3 are scored (the rankability cut is ≥ 3 of 5); the pre-treatment composite is the renormalised mean over the scored axes, raw_burden = 0.6833. The registry-grade [L] axes here are onset and progression (onset from the Orphanet AverageAgeOfOnset register / HPO). Mortality remains an [H] inference from the cited clinical definition.

Because those axes carry [H] inferences, this position is a provisional [H] prioritisation device, not a registry-locked ranking.

The natural-history registry passes have been run against Orphanet/Orphadata (CC BY 4.0, R6) and the openly published GBD 2013 disability-weights table (Salomon et al., CC BY, R7). R6 lifts onset to registry-grade [L] across most of the cohort (earliest AverageAgeOfOnset category, entity-anchored per ORPHAcode, Exact OMIM↔ORPHA only); R7 lifts disability to [L] where one dominant untreated sequela maps to a named GBD health state (published disability weight binned by declared cut-points), and independently corroborates a mortality axis from PMC survival literature where a quantitative disease-typical figure exists. Severity now lifts to registry [L] for the one disease whose dominant sequela carries a cited HPO Severity-modifier annotation (the HP:0012824 subtree, R8); for the rest the open HPO severity annotations are feature-level (using one feature as the disease tier would be a category error), so severity stays [H]/[O] with the obstacle named. Progression lifts to registry [L] where a cited PMC open-access source states a disease-level magnitude for the dominant untreated sequela and the frozen R3 tier function derives the tier from that verbatim sentence (R9, curated dominant-sequela join, non-spectrum); for the rest progression stays [H]/[O]. The OMIM clinical synopsis (the disease-level alternative) is API-key-gated and the key is unobtainable for an individual researcher — that path is removed, not guessed.

Established treatment and residual burden

The established disease-directed approach is CFTR modulator therapy (corrector + potentiator) with airway clearance and pancreatic enzyme replacement. Mechanistically: CFTR modulators restore folding and channel gating of mutant CFTR protein [L].

Its effect on natural history is classified disease-modifying (substantial), mapping to an efficacy offset e = 0.5500 and a residual factor R_treat = 0.4500. Applied to the pre-treatment proxy this gives the residual burden score 0.3075, moving the disease from raw rank 11 to residual rank 17 (shift -6).

Evidence tier: accession-dated to the GeneReviews NBK1250 Management section [L] (initial posting March 26, 2001; last revision August 8, 2024; retrieved 2026-06-18; corroborating term(s): “cftr, modulator, airway, clearance, pancreatic, enzyme, replacement”). The natural-history axis grades remain a mix of [L] (GeneReviews-corroborated) and [H] (definition-only), so the burden order is still provisional.