Mosaic Genome-Wide Paternal Uniparental Disomy disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials

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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:

MalaCards categories:
Global: Fetal diseases Rare diseases

See all MalaCards categories (disease lists)

Orphanet: ⁵⁹

Developmental anomalies during embryogenesis

External Ids:

Orphanet ⁵⁹ ORPHA329813

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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.

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Related Diseases for Mosaic Genome-Wide Paternal Uniparental Disomy

Diseases related to Mosaic Genome-Wide Paternal Uniparental Disomy via text searches within MalaCards or GeneCards Suite gene sharing:

(show all 29)

#	Related Disease	Score
1	congenital heart defects, hamartomas of tongue, and polysyndactyly	10.6
2	paternal uniparental disomy	10.5
3	beckwith-wiedemann syndrome	10.5
4	nephronophthisis 3	10.3
5	autosomal recessive disease	10.3
6	renal-hepatic-pancreatic dysplasia	10.3
7	hemangioma	10.3
8	gestational trophoblastic tumor	10.3
9	ciliopathy	10.3
10	overgrowth syndrome	10.3
11	angelman syndrome	10.3
12	pheochromocytoma	10.3
13	prader-willi syndrome	10.3
14	silver-russell syndrome	10.3
15	hydatidiform mole, recurrent, 1	10.3
16	hyperinsulinemic hypoglycemia, familial, 5	10.3
17	hyperinsulinemic hypoglycemia, familial, 4	10.3
18	adrenal gland pheochromocytoma	10.3
19	transient neonatal diabetes mellitus	10.3
20	neonatal diabetes mellitus	10.3
21	hyperinsulinemic hypoglycemia	10.3
22	breast fibroadenoma	10.3
23	hyperinsulinism	10.3
24	gestational trophoblastic neoplasm	10.3
25	pancreatoblastoma	10.3
26	polyhydramnios	10.3
27	hypoglycemia	10.3
28	diencephalic syndrome	10.3
29	triploidy	10.3

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

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Symptoms & Phenotypes for Mosaic Genome-Wide Paternal Uniparental Disomy

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Drugs & Therapeutics for Mosaic Genome-Wide Paternal Uniparental Disomy

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

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Genetic Tests for Mosaic Genome-Wide Paternal Uniparental Disomy

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Anatomical Context for Mosaic Genome-Wide Paternal Uniparental Disomy

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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	Postema FAM...Hennekam RC	30882989	2019
2	Tissue variations of mosaic genome-wide paternal uniparental disomy and phenotype of multi-syndromal congenital hyperinsulinism. ³⁸	Christesen HT...Detlefsen S	30797057	2019
3	First report of congenital adrenal cysts and pheochromocytoma in a patient with mosaic genome-wide paternal uniparental disomy. ³⁸	White M...Zacharin MR	27734603	2016
4	Genome-wide paternal uniparental disomy mosaicism in a woman with Beckwith-Wiedemann syndrome and ovarian steroid cell tumour. ³⁸	Gogiel M...Strobl-Wildemann G	23188046	2013
5	Mosaicism for genome-wide paternal uniparental disomy with features of multiple imprinting disorders: diagnostic and management issues. ³⁸	Inbar-Feigenberg M...Weksberg R	23239666	2013

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Genes for Mosaic Genome-Wide Paternal Uniparental Disomy

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Variations for Mosaic Genome-Wide Paternal Uniparental Disomy

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Expression for Mosaic Genome-Wide Paternal Uniparental Disomy

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

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Pathways for Mosaic Genome-Wide Paternal Uniparental Disomy

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GO Terms for Mosaic Genome-Wide Paternal Uniparental Disomy

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Sources for Mosaic Genome-Wide Paternal Uniparental Disomy

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