Sjukdomar som orsakas av transkriptionell tystnad av en av föräldrarnas genalleler (imprintad gen). Genetisk prägling visar genetiskt uttryck från endast en förälder i genparet genom epigenetiska processer utan någon förändring i DNA-sekvensen.
Disorders caused by transcriptional silencing of one parental gene allele (imprinted gene). Imprinted genes show genetic expression from only one parent of the gene pair through epigenetic processes with no change in the DNA sequence.
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Disorder, Imprinting — Imprinting Disorder — Genetic Imprinting Disorders — Disorder, Genetic Imprinting — Genetic Imprinting Disorder — Imprinting Disorder, Genetic — Genomic Imprinting Disorders — Disorder, Genomic Imprinting — Genomic Imprinting Disorder — Imprinting Disorder, Genomic — Imprinting Diseases — Disease, Imprinting — Imprinting Disease — Imprinting Syndromes — Imprinting Syndrome — Syndrome, Imprinting