Terminology Service for NFDI4Health
autosomal inheritance
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http://purl.obolibrary.org/obo/GENO_0000934
An inheritance pattern wherein the trait is determined by alleles of a single causal gene on a non-sex chromosome.
Term info
Label
autosomal inheritance
Term relations
Related from:
has material basis in
- hypophosphatasia
- Robinow syndrome
- McCune Albright syndrome
- Aicardi-Goutieres syndrome
- Matthew-Wood syndrome
- progeria
- familial adenomatous polyposis
- Weill-Marchesani syndrome
- familial Mediterranean fever
- Gillespie syndrome
- hereditary desmoid disease
- exudative vitreoretinopathy 4
- camptodactyly-tall stature-scoliosis-hearing loss syndrome
- blepharophimosis, ptosis, and epicanthus inversus syndrome
- factor XI deficiency
- septooptic dysplasia