MCID: CHR183
MIFTS: 13

Chromosome 10q Deletion

Categories: Rare diseases

Aliases & Classifications for Chromosome 10q Deletion

MalaCards integrated aliases for Chromosome 10q Deletion:

Name: Chromosome 10q Deletion 20
Chromosome 10, Monosomy 10q 70
Partial Monosomy 10q 20
10q Deletion 20
10q Monosomy 20
Deletion 10q 20
Monosomy 10q 20

Classifications:



External Ids:

UMLS 70 C0795839

Summaries for Chromosome 10q Deletion

GARD : 20 Chromosome 10q deletion is a chromosome abnormality that occurs when there is a missing copy of the genetic material located on the long arm (q) of chromosome 10. The severity of the condition and the signs and symptoms depend on the size and location of the deletion and which genes are involved. Features that often occur in people with chromosome 10q deletion include developmental delay, intellectual disability, behavioral problems, and distinctive facial features. Most cases are not inherited, but people can pass the deletion on to their children. Treatment is based on the signs and symptoms present in each person.

MalaCards based summary : Chromosome 10q Deletion, also known as chromosome 10, monosomy 10q, is related to chromosome 10q26 deletion syndrome and 10q26 deletion syndrome. An important gene associated with Chromosome 10q Deletion is DEL10Q26 (Chromosome 10q Deletion Syndrome).

Related Diseases for Chromosome 10q Deletion

Graphical network of the top 20 diseases related to Chromosome 10q Deletion:



Diseases related to Chromosome 10q Deletion

Symptoms & Phenotypes for Chromosome 10q Deletion

Drugs & Therapeutics for Chromosome 10q Deletion

Search Clinical Trials , NIH Clinical Center for Chromosome 10q Deletion

Genetic Tests for Chromosome 10q Deletion

Anatomical Context for Chromosome 10q Deletion

Publications for Chromosome 10q Deletion

Articles related to Chromosome 10q Deletion:

(show all 14)
# Title Authors PMID Year
1
MGMT-Methylated Alleles Are Distributed Heterogeneously Within Glioma Samples Irrespective of IDH Status and Chromosome 10q Deletion. 61
27346749 2016
2
Contribution of 1p, 19q, 9p and 10q Automated Analysis by FISH to the Diagnosis and Prognosis of Oligodendroglial Tumors According to WHO 2016 Guidelines. 61
28030632 2016
3
TERT promoter mutations are highly recurrent in SHH subgroup medulloblastoma. 61
24174164 2013
4
Comprehensive analysis of PTEN status in Sezary syndrome. 61
24062018 2013
5
Chromosome 10q deletion del (10)(q26.1q26.3) is associated with cataract. 61
23590959 2013
6
Rapid aneuploidy diagnosis of partial trisomy 7q (7q34→qter) and partial monosomy 10q (10q26.12→qter) by array comparative genomic hybridization using uncultured amniocytes. 61
22482977 2012
7
Pediatric and adult sonic hedgehog medulloblastomas are clinically and molecularly distinct. 61
21681522 2011
8
[Cytogenetic and molecular characterization of partial trisomy 4q and partial monosomy 10q in a patient]. 61
20376795 2010
9
Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia. 61
15966044 2005
10
Partial monosomy 10q with partial trisomy 11q due to paternal balanced translocation. 61
11328480 2001
11
Point mutation and homozygous deletion of PTEN/MMAC1 in primary bladder cancers. 61
9671402 1998
12
Partial monosomy 10q and partial trisomy 9q with anal atresia due to maternal translocation: t(9;10)(q32;q26). 61
9001803 1996
13
The partial monosomy 10q syndrome: report on two patients and review of the developmental data. 61
1920392 1991
14
Monosomy 10qter due to a balanced maternal translocation: t(10;8)(q23;p23). 61
6616953 1983

Variations for Chromosome 10q Deletion

Expression for Chromosome 10q Deletion

Search GEO for disease gene expression data for Chromosome 10q Deletion.

Pathways for Chromosome 10q Deletion

GO Terms for Chromosome 10q Deletion

Sources for Chromosome 10q Deletion

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-Apr-2021)
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 Tocris
70 UMLS
71 UMLS via Orphanet
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