MCID: DFN091

Dfnx2 Nonsyndromic Hearing Loss and Deafness malady

Categories: Genetic diseases (common), Ear diseases

Aliases & Classifications for Dfnx2 Nonsyndromic Hearing Loss and Deafness

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Aliases & Descriptions for Dfnx2 Nonsyndromic Hearing Loss and Deafness:

Name: Dfnx2 Nonsyndromic Hearing Loss and Deafness 24

Classifications:



Summaries for Dfnx2 Nonsyndromic Hearing Loss and Deafness

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MalaCards based summary: Dfnx2 Nonsyndromic Hearing Loss and Deafness An important gene associated with Dfnx2 Nonsyndromic Hearing Loss and Deafness is POU3F4 (POU Class 3 Homeobox 4).

Related Diseases for Dfnx2 Nonsyndromic Hearing Loss and Deafness

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Symptoms & Phenotypes for Dfnx2 Nonsyndromic Hearing Loss and Deafness

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Drugs & Therapeutics for Dfnx2 Nonsyndromic Hearing Loss and Deafness

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Interventional clinical trials:

Search ClinicalTrials, NIH Clinical Center for Dfnx2 Nonsyndromic Hearing Loss and Deafness

Genetic Tests for Dfnx2 Nonsyndromic Hearing Loss and Deafness

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Genetic tests related to Dfnx2 Nonsyndromic Hearing Loss and Deafness:

id Genetic test Affiliating Genes
1 Dfnx2 Nonsyndromic Hearing Loss and Deafness24 POU3F4

Anatomical Context for Dfnx2 Nonsyndromic Hearing Loss and Deafness

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Publications for Dfnx2 Nonsyndromic Hearing Loss and Deafness

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Variations for Dfnx2 Nonsyndromic Hearing Loss and Deafness

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Expression for genes affiliated with Dfnx2 Nonsyndromic Hearing Loss and Deafness

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Search GEO for disease gene expression data for Dfnx2 Nonsyndromic Hearing Loss and Deafness.

Pathways for genes affiliated with Dfnx2 Nonsyndromic Hearing Loss and Deafness

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GO Terms for genes affiliated with Dfnx2 Nonsyndromic Hearing Loss and Deafness

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Sources for Dfnx2 Nonsyndromic Hearing Loss and Deafness

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2CDC
6CNVD
10DGIdb
15ExPASy
16FDA
17FMA
27GTR
28HGMD
29HMDB
30ICD10
31ICD10 via Orphanet
32ICD9CM
33IUPHAR
34KEGG
37MedGen
39MeSH
40MESH via Orphanet
41MGI
44NCI
45NCIt
46NDF-RT
49NINDS
50Novoseek
52OMIM
53OMIM via Orphanet
57PubMed
58QIAGEN
63SNOMED-CT via Orphanet
67Tumor Gene Family of Databases
68UMLS
69UMLS via Orphanet