Autosomal recessive inheritance SNOMEDCT_US:258211005 Autosomal recessive Autosomal recessive predisposition UMLS:C0441748 HP:0031362 Autosomal recessive form HP:0000007 HP:0001416 HP:0001526 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 individuals with two pathogenic alleles, either homozygotes (two copies of the same mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele). UMLS:C4020899 biallelic_autosomal Mendelian inheritance