MCID: SYN137
MIFTS: 8

Syndromic Genetic Deafness

Categories: Ear diseases, Fetal diseases, Rare diseases

Aliases & Classifications for Syndromic Genetic Deafness

MalaCards integrated aliases for Syndromic Genetic Deafness:

Name: Syndromic Genetic Deafness 58

Classifications:

Orphanet: 58  
Rare otorhinolaryngological diseases
Developmental anomalies during embryogenesis


External Ids:

ICD10 via Orphanet 33 H90.3
Orphanet 58 ORPHA90642

Summaries for Syndromic Genetic Deafness

Related Diseases for Syndromic Genetic Deafness

Diseases related to Syndromic Genetic Deafness via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 non-syndromic genetic deafness 12.2
2 deafness, conductive, with malformed external ear 11.0
3 knuckle pads, leuconychia and sensorineural deafness 11.0
4 branchiootic syndrome 1 9.9
5 pendred syndrome 9.7
6 ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus 9.7

Graphical network of the top 20 diseases related to Syndromic Genetic Deafness:



Diseases related to Syndromic Genetic Deafness

Symptoms & Phenotypes for Syndromic Genetic Deafness

Drugs & Therapeutics for Syndromic Genetic Deafness

Search Clinical Trials , NIH Clinical Center for Syndromic Genetic Deafness

Genetic Tests for Syndromic Genetic Deafness

Anatomical Context for Syndromic Genetic Deafness

Publications for Syndromic Genetic Deafness

Articles related to Syndromic Genetic Deafness:

# Title Authors PMID Year
1
Deafness on the island of Providencia - Colombia: different etiology, different genetic counseling. 61
19239084 2008
2
A novel type of myosin encoded by the mouse deafness gene shaker-2. 61
9703981 1998

Variations for Syndromic Genetic Deafness

Expression for Syndromic Genetic Deafness

Search GEO for disease gene expression data for Syndromic Genetic Deafness.

Pathways for Syndromic Genetic Deafness

GO Terms for Syndromic Genetic Deafness

Sources for Syndromic Genetic Deafness

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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