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The 62 pages that link to Autosomal dominant inheritance, each with the reason it gives.

• Manx catNarrower topic: The Manx tail-length variant is inherited as a dominant trait, with outcomes shaped by gene dosage.

• Rubinstein–Taybi syndromeRelated: The syndrome follows this inheritance pattern, though most cases arise from new variants.

• CADASILNarrower topic: A single pathogenic NOTCH3 variant can cause CADASIL, so the condition may recur across generations.

• CherubismRelated: Cherubism is commonly inherited this way, though new mutations also occur.

• Cleidocranial dysostosisRelated: A person with a RUNX2-related case may pass the variant to each child with a 50% chance.

• Cornelia de Lange syndromeRelated: Most established Cornelia de Lange syndrome gene variants act dominantly, often arising de novo.

• Darier diseaseRelated: Affected individuals commonly have a one-in-two chance of passing the variant to each child.

• Fibrodysplasia ossificans progressivaRelated: The disorder follows this inheritance pattern, although most cases result from new mutations.

• Gerstmann–Sträussler–Scheinker syndromeNarrower topic: A pathogenic PRNP variant can be passed through successive generations in this pattern.

• Stickler syndromeRelated: Most Stickler syndrome forms are inherited this way, though severity can vary within families.

• Treacher Collins syndromeRelated: Many cases result from a dominant variant inherited from a parent or arising for the first time.

• Uncombable hair syndromeCompared with: Some reported families differ from the more commonly described recessive inheritance pattern.