UPD
MCID: CHR180
MIFTS: 16

Chromosome 10, Uniparental Disomy (UPD)

Categories: Fetal diseases, Rare diseases

Aliases & Classifications for Chromosome 10, Uniparental Disomy

MalaCards integrated aliases for Chromosome 10, Uniparental Disomy:

Name: Chromosome 10, Uniparental Disomy 20
Mosaic Trisomy 10 20 58 29
Chromosome 10, Uniparental Disomy of 71
Uniparental Disomy of Chromosome X 58
Mosaic Trisomy Chromosome 10 58
Uniparental Disomy of 10 20
Trisomy 10 Mosaicism 58
Upd 58

Classifications:

Orphanet: 58  
Developmental anomalies during embryogenesis


External Ids:

ICD10 via Orphanet 33 Q92.1 Q99.8
UMLS 71 C2931794

Summaries for Chromosome 10, Uniparental Disomy

MalaCards based summary : Chromosome 10, Uniparental Disomy, also known as mosaic trisomy 10, is related to paternal uniparental disomy of chromosome x and maternal uniparental disomy of chromosome x.

Related Diseases for Chromosome 10, Uniparental Disomy

Diseases in the Uniparental Disomy of Chromosome 1 family:

Chromosome 1, Uniparental Disomy 1q12 Q21 Chromosome 10, Uniparental Disomy
Chromosome 16, Uniparental Disomy Chromosome 21, Uniparental Disomy
Chromosome 5, Uniparental Disomy Uniparental Disomy of Chromosome 11
Uniparental Disomy of Chromosome 2 Uniparental Disomy of Chromosome 6
Uniparental Disomy of Chromosome 15 Uniparental Disomy of Chromosome 20
Uniparental Disomy of Chromosome 13 Uniparental Disomy of Chromosome 14
Uniparental Disomy of Chromosome 7

Diseases related to Chromosome 10, Uniparental Disomy via text searches within MalaCards or GeneCards Suite gene sharing:

(show top 50) (show all 145)
# Related Disease Score Top Affiliating Genes
1 paternal uniparental disomy of chromosome x 11.4
2 maternal uniparental disomy of chromosome x 11.4
3 mulchandani-bhoj-conlin syndrome 11.1
4 uniparental disomy of chromosome 6 11.1
5 paternal uniparental disomy of chromosome 20 11.0
6 prader-willi syndrome 11.0
7 kagami-ogata syndrome 10.9
8 uniparental disomy of chromosome 7 10.9
9 uniparental disomy of chromosome 2 10.9
10 maternal uniparental disomy of chromosome 16 10.9
11 uniparental disomy of chromosome 15 10.9
12 uniparental disomy of chromosome 14 10.9
13 maternal uniparental disomy of chromosome 6 10.9
14 uniparental disomy of chromosome 1 10.9
15 temple syndrome 10.8
16 chromosome 16, uniparental disomy 10.8
17 chromosome 21, uniparental disomy 10.8
18 uniparental disomy of chromosome 11 10.8
19 paternal uniparental disomy of chromosome 1 10.8
20 maternal uniparental disomy of chromosome 1 10.8
21 uniparental disomy of chromosome 20 10.8
22 uniparental disomy of chromosome 13 10.8
23 silver-russell syndrome due to maternal uniparental disomy of chromosome 11 10.8
24 mosaic genome-wide paternal uniparental disomy 10.8
25 maternal uniparental disomy of chromosome 9 10.8
26 silver-russell syndrome due to maternal uniparental disomy of chromosome 7 10.8
27 maternal uniparental disomy of chromosome 4 10.8
28 maternal uniparental disomy of chromosome 2 10.8
29 paternal uniparental disomy of chromosome 6 10.8
30 paternal uniparental disomy of chromosome 5 10.8
31 maternal uniparental disomy of chromosome 22 10.8
32 maternal uniparental disomy of chromosome 21 10.8
33 paternal uniparental disomy of chromosome 21 10.8
34 paternal uniparental disomy of chromosome 7 10.8
35 beckwith-wiedemann syndrome due to paternal uniparental disomy of chromosome 11 10.8
36 maternal uniparental disomy of chromosome 13 10.8
37 paternal uniparental disomy of chromosome 13 10.8
38 angelman syndrome due to paternal uniparental disomy of chromosome 15 10.8
39 maternal uniparental disomy 10.5
40 chromosomal triplication 10.4
41 silver-russell syndrome 1 10.3
42 diencephalic syndrome 10.3
43 paternal uniparental disomy 10.3
44 angelman syndrome 10.2
45 hypotonia 10.2
46 alacrima, achalasia, and mental retardation syndrome 10.1
47 47,xyy 10.1
48 hypertelorism 10.1
49 cleft lip/palate 10.1
50 autosomal recessive disease 10.1

Graphical network of the top 20 diseases related to Chromosome 10, Uniparental Disomy:



Diseases related to Chromosome 10, Uniparental Disomy

Symptoms & Phenotypes for Chromosome 10, Uniparental Disomy

Drugs & Therapeutics for Chromosome 10, Uniparental Disomy

Search Clinical Trials , NIH Clinical Center for Chromosome 10, Uniparental Disomy

Genetic Tests for Chromosome 10, Uniparental Disomy

Genetic tests related to Chromosome 10, Uniparental Disomy:

# Genetic test Affiliating Genes
1 Mosaic Trisomy 10 29

Anatomical Context for Chromosome 10, Uniparental Disomy

Publications for Chromosome 10, Uniparental Disomy

Articles related to Chromosome 10, Uniparental Disomy:

# Title Authors PMID Year
1
Prenatal diagnosis of bilateral ectrodactyly and radial agenesis associated with trisomy 10 mosaicism. 61
23401811 2013
2
Novel mutation of the perforin gene and maternal uniparental disomy 10 in a patient with familial hemophagocytic lymphohistiocytosis. 61
18799942 2008
3
Identification of a case of maternal uniparental disomy of chromosome 10 associated with confined placental mosaicism. 61
8559755 1995

Variations for Chromosome 10, Uniparental Disomy

Expression for Chromosome 10, Uniparental Disomy

Search GEO for disease gene expression data for Chromosome 10, Uniparental Disomy.

Pathways for Chromosome 10, Uniparental Disomy

GO Terms for Chromosome 10, Uniparental Disomy

Sources for Chromosome 10, Uniparental Disomy

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
20 GARD
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
53 NINDS
54 Novoseek
56 OMIM via Orphanet
57 OMIM® (Updated 05-Mar-2021)
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
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