MCID: PTR021
MIFTS: 4

Paternal Uniparental Disomy of Chromosome 21

Categories: Fetal diseases, Rare diseases

Aliases & Classifications for Paternal Uniparental Disomy of Chromosome 21

MalaCards integrated aliases for Paternal Uniparental Disomy of Chromosome 21:

Name: Paternal Uniparental Disomy of Chromosome 21 58
Upd(21)pat 58

Classifications:

Orphanet: 58  
Developmental anomalies during embryogenesis


External Ids:

ICD10 via Orphanet 33 Q99.8
Orphanet 58 ORPHA96195

Summaries for Paternal Uniparental Disomy of Chromosome 21

MalaCards based summary : Paternal Uniparental Disomy of Chromosome 21, is also known as upd(21)pat.

Related Diseases for Paternal Uniparental Disomy of Chromosome 21

Symptoms & Phenotypes for Paternal Uniparental Disomy of Chromosome 21

Drugs & Therapeutics for Paternal Uniparental Disomy of Chromosome 21

Search Clinical Trials , NIH Clinical Center for Paternal Uniparental Disomy of Chromosome 21

Genetic Tests for Paternal Uniparental Disomy of Chromosome 21

Anatomical Context for Paternal Uniparental Disomy of Chromosome 21

Publications for Paternal Uniparental Disomy of Chromosome 21

Variations for Paternal Uniparental Disomy of Chromosome 21

Expression for Paternal Uniparental Disomy of Chromosome 21

Search GEO for disease gene expression data for Paternal Uniparental Disomy of Chromosome 21.

Pathways for Paternal Uniparental Disomy of Chromosome 21

GO Terms for Paternal Uniparental Disomy of Chromosome 21

Sources for Paternal Uniparental Disomy of Chromosome 21

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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