MCID: DFN084
MIFTS: 4

Dfnb49 Nonsyndromic Hearing Loss and Deafness

Categories: Genetic diseases, Ear diseases

Aliases & Classifications for Dfnb49 Nonsyndromic Hearing Loss and Deafness

MalaCards integrated aliases for Dfnb49 Nonsyndromic Hearing Loss and Deafness:

Name: Dfnb49 Nonsyndromic Hearing Loss and Deafness 24
Dfnb 49 Nonsyndromic Hearing Loss and Deafness 24

Classifications:



Summaries for Dfnb49 Nonsyndromic Hearing Loss and Deafness

MalaCards based summary : Dfnb49 Nonsyndromic Hearing Loss and Deafness, is also known as dfnb 49 nonsyndromic hearing loss and deafness. An important gene associated with Dfnb49 Nonsyndromic Hearing Loss and Deafness is MARVELD2 (MARVEL Domain Containing 2).

Related Diseases for Dfnb49 Nonsyndromic Hearing Loss and Deafness

Symptoms & Phenotypes for Dfnb49 Nonsyndromic Hearing Loss and Deafness

Drugs & Therapeutics for Dfnb49 Nonsyndromic Hearing Loss and Deafness

Search Clinical Trials , NIH Clinical Center for Dfnb49 Nonsyndromic Hearing Loss and Deafness

Genetic Tests for Dfnb49 Nonsyndromic Hearing Loss and Deafness

Genetic tests related to Dfnb49 Nonsyndromic Hearing Loss and Deafness:

id Genetic test Affiliating Genes
1 Dfnb49 Nonsyndromic Hearing Loss and Deafness 24 MARVELD2

Anatomical Context for Dfnb49 Nonsyndromic Hearing Loss and Deafness

Publications for Dfnb49 Nonsyndromic Hearing Loss and Deafness

Variations for Dfnb49 Nonsyndromic Hearing Loss and Deafness

Expression for Dfnb49 Nonsyndromic Hearing Loss and Deafness

Search GEO for disease gene expression data for Dfnb49 Nonsyndromic Hearing Loss and Deafness.

Pathways for Dfnb49 Nonsyndromic Hearing Loss and Deafness

GO Terms for Dfnb49 Nonsyndromic Hearing Loss and Deafness

Sources for Dfnb49 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 HPO
66 SNOMED-CT via Orphanet
67 TGDB
68 Tocris
69 UMLS
70 UMLS via Orphanet
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