MCID: MSC084
MIFTS: 11

Mosaic Genome-Wide Paternal Uniparental Disomy

Categories: Fetal diseases, Rare diseases

Aliases & Classifications for Mosaic Genome-Wide Paternal Uniparental Disomy

MalaCards integrated aliases for Mosaic Genome-Wide Paternal Uniparental Disomy:

Name: Mosaic Genome-Wide Paternal Uniparental Disomy 59
Genome-Wide Paternal Uniparental Disomy Mosaicism 59
Androgenetic/biparental Mosaicism 59
Mosaic Genome-Wide Paternal Upd 59

Classifications:



External Ids:

Orphanet 59 ORPHA329813

Summaries for Mosaic Genome-Wide Paternal Uniparental Disomy

MalaCards based summary : Mosaic Genome-Wide Paternal Uniparental Disomy, also known as genome-wide paternal uniparental disomy mosaicism, is related to congenital heart defects, hamartomas of tongue, and polysyndactyly and paternal uniparental disomy.

Related Diseases for Mosaic Genome-Wide Paternal Uniparental Disomy

Graphical network of the top 20 diseases related to Mosaic Genome-Wide Paternal Uniparental Disomy:



Diseases related to Mosaic Genome-Wide Paternal Uniparental Disomy

Symptoms & Phenotypes for Mosaic Genome-Wide Paternal Uniparental Disomy

Drugs & Therapeutics for Mosaic Genome-Wide Paternal Uniparental Disomy

Search Clinical Trials , NIH Clinical Center for Mosaic Genome-Wide Paternal Uniparental Disomy

Genetic Tests for Mosaic Genome-Wide Paternal Uniparental Disomy

Anatomical Context for Mosaic Genome-Wide Paternal Uniparental Disomy

Publications for Mosaic Genome-Wide Paternal Uniparental Disomy

Articles related to Mosaic Genome-Wide Paternal Uniparental Disomy:

# Title Authors PMID Year
1
Multiple tumors due to mosaic genome-wide paternal uniparental disomy. 38
30882989 2019
2
Tissue variations of mosaic genome-wide paternal uniparental disomy and phenotype of multi-syndromal congenital hyperinsulinism. 38
30797057 2019
3
First report of congenital adrenal cysts and pheochromocytoma in a patient with mosaic genome-wide paternal uniparental disomy. 38
27734603 2016
4
Genome-wide paternal uniparental disomy mosaicism in a woman with Beckwith-Wiedemann syndrome and ovarian steroid cell tumour. 38
23188046 2013
5
Mosaicism for genome-wide paternal uniparental disomy with features of multiple imprinting disorders: diagnostic and management issues. 38
23239666 2013

Variations for Mosaic Genome-Wide Paternal Uniparental Disomy

Expression for Mosaic Genome-Wide Paternal Uniparental Disomy

Search GEO for disease gene expression data for Mosaic Genome-Wide Paternal Uniparental Disomy.

Pathways for Mosaic Genome-Wide Paternal Uniparental Disomy

GO Terms for Mosaic Genome-Wide Paternal Uniparental Disomy

Sources for Mosaic Genome-Wide Paternal Uniparental Disomy

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 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 TGDB
71 Tocris
72 UMLS
73 UMLS via Orphanet
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