Paternal uniparental disomy of chromosome 6

MONDO:0019921

Paternal uniparental disomy of chromosome 6 is an uniparental disomy of paternal origin characterized by intrauterine growth retardation, transient neonatal diabetes mellitus, and macroglossia.

Also known as: UPD(6)pat, paternal uniparental disomy of chromosome type 6

0 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Disease (680) Human disease (14) Chromosomal disorder (12) Disease of genetic or genomic mechanism (2) Autosomal anomaly (0) Chromosome 6 disorder (0) Disease by etiologic mechanism (0) Uniparental disomy (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.