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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Mendelian inheritance +     
Autosomal dominant inheritance  
A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele.
Autosomal recessive inheritance  
Mitochondrial inheritance  
Pseudoautosomal inheritance +  
Semidominant inheritance 
X-linked inheritance +   
Y-linked inheritance  

Synonyms
Exact Synonyms: Autosomal dominant ;   monoallelic_autosomal
Related Synonyms: AUTOSOMAL DOMINANT FORM ;   AUTOSOMAL DOMINANT TYPE
Alternate IDs: HP:0001415 ;   HP:0001447 ;   HP:0001448 ;   HP:0001451 ;   HP:0001452 ;   HP:0001455 ;   HP:0001456 ;   HP:0001463
Xrefs: SNOMEDCT_US:263681008 ;   UMLS:C0443147
Definition Sources: https://orcid.org/0000-0002-0736-9199

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