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The 70 pages that link to Autosomal recessive inheritance, each with the reason it gives.

• Genetic counselingRelated: This pattern frames carrier results and reproductive risk discussions.

• Newborn screeningRelated: Many screened genetic disorders follow this inheritance pattern.

• Sickle cell diseaseRelated: Most forms require disease-associated globin variants from both parents.

• Retinitis pigmentosaRelated: Many affected people have no family history because relatives may carry one variant.

• Genetic disorderRelated: Carriers can pass on an altered gene without having the disorder themselves.

• Wilson's diseaseRelated: Wilson's disease usually develops when pathogenic ATP7B variants are inherited from both parents.

• Spinal muscular atrophyRelated: Most common spinal muscular atrophy results from inheriting affected SMN1 copies from both parents.

• LeukodystrophyRelated: Many leukodystrophies follow this inheritance pattern, though other patterns also occur.

• Alport syndromeRelated: Biallelic COL4A3 or COL4A4 variants can cause severe Alport syndrome.

• Congenital myopathyRelated: Many congenital myopathies occur when both gene copies are affected.

• Gaucher diseaseRelated: Gaucher disease typically requires pathogenic variants in both GBA1 copies.

• Bardet–Biedl syndromeRelated: Most cases arise when a person inherits an altered BBS gene copy from each parent.

• Crigler–Najjar syndromeRelated: Crigler–Najjar syndrome typically develops when both UGT1A1 copies carry pathogenic variants.

• CystinuriaRelated: This pattern commonly describes cystinuria caused by SLC3A1 variants.

• Tay–Sachs diseaseRelated: Tay–Sachs disease typically develops when a person inherits pathogenic HEXA variants from both parents.

• Krabbe diseaseRelated: Krabbe disease is usually inherited when a child receives a nonworking GALC copy from each parent.

• Leber congenital amaurosisRelated: Most cases result from pathogenic variants inherited in two copies of a gene.

• Maple syrup urine diseaseRelated: Affected children typically inherit one disease-causing variant from each carrier parent.

• Xeroderma pigmentosumRelated: Most XP forms follow this pattern, shaping recurrence risks within families.

• Bloom syndromeRelated: Bloom syndrome usually requires a disease-causing BLM variant from each parent.

• Canavan diseaseRelated: Canavan disease generally requires pathogenic ASPA variants from both parents.

• Charcot–Marie–Tooth diseaseRelated: Some CMT forms appear when a person inherits disease-causing variants from both parents.

• Cockayne syndromeRelated: Cockayne syndrome generally requires disease-causing variants in both copies of an associated gene.

• Fanconi anemiaRelated: Most Fanconi anemia forms follow this inheritance pattern.

• GalactosemiaRelated: Most forms of galactosemia follow this pattern, giving carrier parents a 25% recurrence risk per pregnancy.

• Gitelman syndromeRelated: Gitelman syndrome typically requires pathogenic variants in both copies of SLC12A3.

• Leigh syndromeRelated: Many nuclear-gene forms of Leigh syndrome follow this inheritance pattern.

• Rotor syndromeRelated: Rotor syndrome requires pathogenic changes affecting both transporter genes.

• AlkaptonuriaRelated: Alkaptonuria typically develops when pathogenic HGD variants are inherited from both parents.

• Alström syndromeRelated: Alström syndrome usually occurs when a child inherits one altered ALMS1 copy from each parent.

• HeterozygousRelated: Heterozygotes often carry one pathogenic variant without having the recessive condition.

• Joubert syndromeRelated: Most Joubert syndrome cases result from two disease-causing variants in a single gene.

• TrimethylaminuriaRelated: The inherited form commonly appears when both FMO3 gene copies are impaired.

• AbetalipoproteinemiaRelated: Abetalipoproteinemia usually requires pathogenic variants in both copies of MTTP.

• Amelogenesis imperfectaRelated: Other forms appear when a child inherits disease-causing variants from each parent.

• Familial Mediterranean feverRelated: Most cases follow this pattern, though some people with one pathogenic MEFV variant develop symptoms.

• Glycogen storage disease type VRelated: McArdle disease typically results from pathogenic variants in both copies of PYGM.

• Harlequin ichthyosisRelated: Harlequin ichthyosis typically requires pathogenic ABCA12 variants from both parents.

• HomozygousRelated: Homozygosity for a disease-associated variant can produce this inheritance pattern.

• Tangier diseaseRelated: Tangier disease typically requires disease-causing ABCA1 variants on both gene copies.

• Urbach–Wiethe diseaseRelated: The disorder typically develops when both inherited copies of ECM1 are affected.

• Werner syndromeRelated: Werner syndrome usually requires pathogenic WRN variants on both gene copies.

• Farber diseaseRelated: Farber disease generally requires pathogenic variants inherited in both copies of ASAH1.

• Hereditary haemochromatosisRelated: Common HFE-related disease usually follows this inheritance pattern.

• Sanfilippo syndromeRelated: Sanfilippo syndrome is generally inherited when a child receives a disease-causing variant from each parent.

• Stargardt diseaseRelated: The common ABCA4-associated form follows this inheritance pattern.

• Tetra-amelia syndromeRelated: Many reported cases follow this inheritance pattern.

• Uncombable hair syndromeRelated: Many inherited cases arise when both copies of a relevant hair-shaft gene carry variants.

• Zellweger syndromeRelated: Zellweger syndrome usually occurs when a child inherits affected PEX gene copies from both parents.