MCID: DFN091
MIFTS: 3

Dfnx2 Nonsyndromic Hearing Loss and Deafness malady

Categories: Genetic diseases, Ear diseases

Aliases & Classifications for Dfnx2 Nonsyndromic Hearing Loss and Deafness

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

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

Symptoms & Phenotypes for Dfnx2 Nonsyndromic Hearing Loss and Deafness

Drugs & Therapeutics for Dfnx2 Nonsyndromic Hearing Loss and Deafness

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

Genetic Tests for Dfnx2 Nonsyndromic Hearing Loss and Deafness

Genetic tests related to Dfnx2 Nonsyndromic Hearing Loss and Deafness:

id Genetic test Affiliating Genes
1 Dfnx2 Nonsyndromic Hearing Loss and Deafness 24 POU3F4

Anatomical Context for Dfnx2 Nonsyndromic Hearing Loss and Deafness

Publications for Dfnx2 Nonsyndromic Hearing Loss and Deafness

Variations for Dfnx2 Nonsyndromic Hearing Loss and Deafness

Expression for Dfnx2 Nonsyndromic Hearing Loss and Deafness

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

Pathways for Dfnx2 Nonsyndromic Hearing Loss and Deafness

GO Terms for Dfnx2 Nonsyndromic Hearing Loss and Deafness

Sources for Dfnx2 Nonsyndromic Hearing Loss and Deafness

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 Orphanet
67 TGDB
68 Tocris
69 UMLS
70 UMLS via Orphanet
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