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 58
Genome-Wide Paternal Uniparental Disomy Mosaicism 58
Androgenetic/biparental Mosaicism 58
Mosaic Genome-Wide Paternal Upd 58

Classifications:

Orphanet: 58  
Developmental anomalies during embryogenesis


External Ids:

Orphanet 58 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
Tissue variations of mosaic genome-wide paternal uniparental disomy and phenotype of multi-syndromal congenital hyperinsulinism. 61
30797057 2020
2
Multiple tumors due to mosaic genome-wide paternal uniparental disomy. 61
30882989 2019
3
First report of congenital adrenal cysts and pheochromocytoma in a patient with mosaic genome-wide paternal uniparental disomy. 61
27734603 2016
4
Genome-wide paternal uniparental disomy mosaicism in a woman with Beckwith-Wiedemann syndrome and ovarian steroid cell tumour. 61
23188046 2013
5
Mosaicism for genome-wide paternal uniparental disomy with features of multiple imprinting disorders: diagnostic and management issues. 61
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 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
43 MeSH
44 MESH via Orphanet
45 MGI
48 NCI
49 NCIt
50 NDF-RT
53 NINDS
54 Novoseek
56 OMIM
57 OMIM via Orphanet
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
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