MCID: KCN003
MIFTS: 5

Kcnj10-Related Pendred Syndrome

Categories: Genetic diseases, Rare diseases, Ear diseases, Endocrine diseases, Fetal diseases

Aliases & Classifications for Kcnj10-Related Pendred Syndrome

MalaCards integrated aliases for Kcnj10-Related Pendred Syndrome:

Name: Kcnj10-Related Pendred Syndrome 24

Classifications:



Summaries for Kcnj10-Related Pendred Syndrome

MalaCards based summary : Kcnj10-Related Pendred Syndrome An important gene associated with Kcnj10-Related Pendred Syndrome is KCNJ10 (Potassium Voltage-Gated Channel Subfamily J Member 10).

Related Diseases for Kcnj10-Related Pendred Syndrome

Diseases in the Pendred Syndrome family:

Foxi1-Related Pendred Syndrome Kcnj10-Related Pendred Syndrome
Slc26a4-Related Pendred Syndrome

Symptoms & Phenotypes for Kcnj10-Related Pendred Syndrome

Drugs & Therapeutics for Kcnj10-Related Pendred Syndrome

Search Clinical Trials , NIH Clinical Center for Kcnj10-Related Pendred Syndrome

Genetic Tests for Kcnj10-Related Pendred Syndrome

Genetic tests related to Kcnj10-Related Pendred Syndrome:

id Genetic test Affiliating Genes
1 Kcnj10-Related Pendred Syndrome 24 KCNJ10

Anatomical Context for Kcnj10-Related Pendred Syndrome

Publications for Kcnj10-Related Pendred Syndrome

Variations for Kcnj10-Related Pendred Syndrome

Expression for Kcnj10-Related Pendred Syndrome

Search GEO for disease gene expression data for Kcnj10-Related Pendred Syndrome.

Pathways for Kcnj10-Related Pendred Syndrome

GO Terms for Kcnj10-Related Pendred Syndrome

Sources for Kcnj10-Related Pendred Syndrome

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
16 ExPASy
18 FMA
28 GO
29 GTR
30 HGMD
31 HMDB
32 HPO
33 ICD10
34 ICD10 via Orphanet
35 ICD9CM
36 IUPHAR
37 KEGG
38 LifeMap
40 MedGen
42 MeSH
43 MESH via Orphanet
44 MGI
46 NCI
47 NCIt
48 NDF-RT
51 NINDS
52 Novoseek
54 OMIM
55 OMIM via Orphanet
59 PubMed
60 QIAGEN
65 SNOMED-CT via HPO
66 SNOMED-CT via Orphanet
67 TGDB
68 Tocris
69 UMLS
70 UMLS via Orphanet
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