autosomal dominant disease (Q21252): Difference between revisions

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Created claim: exact match (P409): http://purl.obolibrary.org/obo/DOID_0050736
Created claim: exact match (P409): http://identifiers.org/doid/DOID:0050736
 
Property / exact match
 
Property / exact match: http://identifiers.org/doid/DOID:0050736 / rank
 
Normal rank

Latest revision as of 10:33, 28 February 2024

genetic disease characterized by the presence of one disease-associated mutation of a gene which is sufficient to cause the disease
  • autosomal dominant inherited disorder
  • autosomal dominant hereditary disorder
  • disease, autosomal dominant
Language Label Description Also known as
English
autosomal dominant disease
genetic disease characterized by the presence of one disease-associated mutation of a gene which is sufficient to cause the disease
  • autosomal dominant inherited disorder
  • autosomal dominant hereditary disorder
  • disease, autosomal dominant

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