MCID: CNG359
MIFTS: 6

Congenitally Uncorrected Transposition of the Great Arteries with Coarctation

Categories: Cardiovascular diseases, Fetal diseases, Rare diseases

Aliases & Classifications for Congenitally Uncorrected Transposition of the Great Arteries with...

MalaCards integrated aliases for Congenitally Uncorrected Transposition of the Great Arteries with Coarctation:

Name: Congenitally Uncorrected Transposition of the Great Arteries with Coarctation 60
Congenitally Uncorrected Transposition of the Great Vessels with Coarctation 60
Tga with Coarctation 60

Characteristics:

Orphanet epidemiological data:

60
congenitally uncorrected transposition of the great arteries with coarctation
Inheritance: Multigenic/multifactorial,Not applicable; Age of onset: Infancy,Neonatal;

Classifications:



External Ids:

ICD10 via Orphanet 35 Q20.3
Orphanet 60 ORPHA99042

Summaries for Congenitally Uncorrected Transposition of the Great Arteries with...

MalaCards based summary : Congenitally Uncorrected Transposition of the Great Arteries with Coarctation, is also known as congenitally uncorrected transposition of the great vessels with coarctation. An important gene associated with Congenitally Uncorrected Transposition of the Great Arteries with Coarctation is CFC1 (Cripto, FRL-1, Cryptic Family 1).

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Variations for Congenitally Uncorrected Transposition of the Great Arteries with...

Expression for Congenitally Uncorrected Transposition of the Great Arteries with...

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GO Terms for Congenitally Uncorrected Transposition of the Great Arteries with...

Sources for Congenitally Uncorrected Transposition of the Great Arteries with...

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
20 FMA
29 GO
30 GTR
31 HGMD
32 HMDB
33 HPO
34 ICD10
35 ICD10 via Orphanet
36 ICD9CM
37 IUPHAR
38 KEGG
39 LifeMap
41 LOVD
43 MedGen
45 MeSH
46 MESH via Orphanet
47 MGI
50 NCI
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52 NDF-RT
55 NINDS
56 Novoseek
58 OMIM
59 OMIM via Orphanet
63 PubMed
65 QIAGEN
70 SNOMED-CT via HPO
71 SNOMED-CT via Orphanet
72 TGDB
73 Tocris
74 UMLS
75 UMLS via Orphanet
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