Uniparental disomy
MONDO:0700086A condition characterized by the inheritance of a chromosome pair from one parent and no chromosomal copies from the other parent. It results in developmental abnormalities or rare recessive disorders.
3 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Paternal uniparental disomy of chromosome 14
(1)
Angelman syndrome due to paternal uniparental disomy of chromosome 15
(0)
Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11
(0)
Maternal uniparental disomy of chromosome 1
(0)
Maternal uniparental disomy of chromosome 13
(0)
Maternal uniparental disomy of chromosome 14
(0)
Maternal uniparental disomy of chromosome 16
(0)
Maternal uniparental disomy of chromosome 2
(0)
Maternal uniparental disomy of chromosome 20
(0)
Maternal uniparental disomy of chromosome 21
(0)
Maternal uniparental disomy of chromosome 22
(0)
Maternal uniparental disomy of chromosome 4
(0)
Maternal uniparental disomy of chromosome 6
(0)
Maternal uniparental disomy of chromosome 9
(0)
Maternal uniparental disomy of chromosome X
(0)
Mosaic genome-wide paternal uniparental disomy
(0)
Paternal uniparental disomy of chromosome 1
(0)
Paternal uniparental disomy of chromosome 13
(0)
Paternal uniparental disomy of chromosome 20
(0)
Paternal uniparental disomy of chromosome 21
(0)