MCID: CHR180
MIFTS: 12

Chromosome 10, Uniparental Disomy

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 53
Chromosome 10, Uniparental Disomy of 29 73
Mosaic Trisomy 10 53 59
Mosaic Trisomy Chromosome 10 59
Uniparental Disomy of 10 53
Trisomy 10 Mosaicism 59

Classifications:



External Ids:

Orphanet 59 ORPHA96063
ICD10 via Orphanet 34 Q92.1
UMLS 73 C2931794

Summaries for Chromosome 10, Uniparental Disomy

MalaCards based summary : Chromosome 10, Uniparental Disomy, also known as chromosome 10, uniparental disomy of, is related to split-hand/foot malformation 1 and chromosomal triplication.

Related Diseases for Chromosome 10, Uniparental Disomy

Diseases in the Chromosome 5, Uniparental Disomy family:

Chromosome 10, Uniparental Disomy Chromosome 16, Uniparental Disomy
Chromosome 21, Uniparental Disomy Uniparental Disomy of Chromosome 11
Uniparental Disomy of Chromosome 2

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

# Related Disease Score Top Affiliating Genes
1 split-hand/foot malformation 1 9.9
2 chromosomal triplication 9.9
3 isolated split hand-split foot malformation 9.9

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 Chromosome 10, Uniparental Disomy of 29

Anatomical Context for Chromosome 10, Uniparental Disomy

Publications for Chromosome 10, Uniparental Disomy

Articles related to Chromosome 10, Uniparental Disomy:

# Title Authors Year
1
Prenatal diagnosis of bilateral ectrodactyly and radial agenesis associated with trisomy 10 mosaicism. ( 23401811 )
2013
2
Partial trisomy 10 mosaicism with cutaneous manifestations: report of a case and review of the literature. ( 9007335 )
1996

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 ExPASy
19 FMA
28 GO
29 GTR
30 HGMD
31 HMDB
32 HPO
33 ICD10
34 ICD10 via Orphanet
35 ICD9CM
36 IUPHAR
37 KEGG
38 LifeMap
40 LOVD
42 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
54 NINDS
55 Novoseek
57 OMIM
58 OMIM via Orphanet
62 PubMed
64 QIAGEN
69 SNOMED-CT via HPO
70 SNOMED-CT via Orphanet
71 TGDB
72 Tocris
73 UMLS
74 UMLS via Orphanet
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