KnowraAutosomal recessive inheritanceLinked fromLinked fromThe 70 pages that link to Autosomal recessive inheritance, each with the reason it gives.All 70Broader topic 5Related 49Narrower topic 9Compared with 7Cystic fibrosisNarrower topic: Cystic fibrosis usually develops when both inherited CFTR copies carry disease-causing variants.Ataxia–telangiectasiaNarrower topic: Ataxia–telangiectasia generally requires pathogenic ATM variants inherited from both parents.CystinosisNarrower topic: Cystinosis usually develops when a person inherits a disease-causing CTNS variant from each parent.Metachromatic leukodystrophyNarrower topic: Most cases arise when both inherited copies of ARSA or PSAP are affected.Usher syndromeNarrower topic: Most Usher syndrome forms follow this inheritance pattern.Wolfram syndromeNarrower topic: Most Wolfram syndrome forms are inherited in this manner.Glycogen storage disease type IINarrower topic: Pompe disease typically develops when a person inherits affected GAA copies from both parents.Rothmund–Thomson syndromeNarrower topic: Both RECQL4- and ANAPC1-related forms generally require two altered gene copies.Smith–Lemli–Opitz syndromeNarrower topic: A child typically develops the syndrome after inheriting a pathogenic DHCR7 variant from each parent.