MCID: SLV016
MIFTS: 7

Silver-Russell Syndrome Due to 7p11.2p13 Microduplication

Categories: Eye diseases, Fetal diseases, Rare diseases

Aliases & Classifications for Silver-Russell Syndrome Due to 7p11.2p13 Microduplication

MalaCards integrated aliases for Silver-Russell Syndrome Due to 7p11.2p13 Microduplication:

Name: Silver-Russell Syndrome Due to 7p11.2p13 Microduplication 58
Silver-Russell Syndrome Due to 7p11.2-P13 Microduplication 58
Silver-Russell Syndrome Due to Trisomy 7p11.2-P13 58
Silver-Russell Syndrome Due to Trisomy 7p11.2p13 58
Silver-Russell Syndrome Due to Dup(7)(p11.2p13) 58

Characteristics:

Orphanet epidemiological data:

58
silver-russell syndrome due to 7p11.2p13 microduplication
Inheritance: Autosomal dominant,Not applicable; Age of onset: Infancy,Neonatal;

Classifications:

Orphanet: 58  
Rare eye diseases
Developmental anomalies during embryogenesis


External Ids:

ICD10 via Orphanet 33 Q87.1
Orphanet 58 ORPHA231137

Summaries for Silver-Russell Syndrome Due to 7p11.2p13 Microduplication

MalaCards based summary : Silver-Russell Syndrome Due to 7p11.2p13 Microduplication, is also known as silver-russell syndrome due to 7p11.2-p13 microduplication. Affiliated tissues include eye.

Related Diseases for Silver-Russell Syndrome Due to 7p11.2p13 Microduplication

Symptoms & Phenotypes for Silver-Russell Syndrome Due to 7p11.2p13 Microduplication

Drugs & Therapeutics for Silver-Russell Syndrome Due to 7p11.2p13 Microduplication

Search Clinical Trials , NIH Clinical Center for Silver-Russell Syndrome Due to 7p11.2p13 Microduplication

Genetic Tests for Silver-Russell Syndrome Due to 7p11.2p13 Microduplication

Anatomical Context for Silver-Russell Syndrome Due to 7p11.2p13 Microduplication

MalaCards organs/tissues related to Silver-Russell Syndrome Due to 7p11.2p13 Microduplication:

40
Eye

Publications for Silver-Russell Syndrome Due to 7p11.2p13 Microduplication

Variations for Silver-Russell Syndrome Due to 7p11.2p13 Microduplication

Expression for Silver-Russell Syndrome Due to 7p11.2p13 Microduplication

Search GEO for disease gene expression data for Silver-Russell Syndrome Due to 7p11.2p13 Microduplication.

Pathways for Silver-Russell Syndrome Due to 7p11.2p13 Microduplication

GO Terms for Silver-Russell Syndrome Due to 7p11.2p13 Microduplication

Sources for Silver-Russell Syndrome Due to 7p11.2p13 Microduplication

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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