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

• 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.

• Recessive traitBroader topic: This is the common inheritance pattern behind many recessive traits and disorders.

• 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.

• Wolfram syndromeNarrower topic: Most Wolfram syndrome forms are inherited in this manner.

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

• Glycogen storage disease type IINarrower topic: Pompe disease typically develops when a person inherits affected GAA copies from both parents.

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

• Rothmund–Thomson syndromeNarrower topic: Both RECQL4- and ANAPC1-related forms generally require two altered gene copies.

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

• Smith–Lemli–Opitz syndromeNarrower topic: A child typically develops the syndrome after inheriting a pathogenic DHCR7 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.

• Treacher Collins syndromeCompared with: Some cases, including those involving POLR1C or POLR1D, follow this pattern rather than dominant inheritance.

• 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.