MCID: DFN072

Dfnb21 Nonsyndromic Hearing Loss and Deafness malady

Categories: Genetic diseases (common), Ear diseases

Aliases & Classifications for Dfnb21 Nonsyndromic Hearing Loss and Deafness

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Aliases & Descriptions for Dfnb21 Nonsyndromic Hearing Loss and Deafness:

Name: Dfnb21 Nonsyndromic Hearing Loss and Deafness 24
 
Dfnb 21 Nonsyndromic Hearing Loss and Deafness 24

Classifications:



Summaries for Dfnb21 Nonsyndromic Hearing Loss and Deafness

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MalaCards based summary: Dfnb21 Nonsyndromic Hearing Loss and Deafness, is also known as dfnb 21 nonsyndromic hearing loss and deafness An important gene associated with Dfnb21 Nonsyndromic Hearing Loss and Deafness is TECTA (Tectorin Alpha).

Related Diseases for Dfnb21 Nonsyndromic Hearing Loss and Deafness

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Symptoms & Phenotypes for Dfnb21 Nonsyndromic Hearing Loss and Deafness

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Drugs & Therapeutics for Dfnb21 Nonsyndromic Hearing Loss and Deafness

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Interventional clinical trials:

Search ClinicalTrials, NIH Clinical Center for Dfnb21 Nonsyndromic Hearing Loss and Deafness

Genetic Tests for Dfnb21 Nonsyndromic Hearing Loss and Deafness

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Genetic tests related to Dfnb21 Nonsyndromic Hearing Loss and Deafness:

id Genetic test Affiliating Genes
1 Dfnb21 Nonsyndromic Hearing Loss and Deafness24 TECTA

Anatomical Context for Dfnb21 Nonsyndromic Hearing Loss and Deafness

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Publications for Dfnb21 Nonsyndromic Hearing Loss and Deafness

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Variations for Dfnb21 Nonsyndromic Hearing Loss and Deafness

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Expression for genes affiliated with Dfnb21 Nonsyndromic Hearing Loss and Deafness

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Search GEO for disease gene expression data for Dfnb21 Nonsyndromic Hearing Loss and Deafness.

Pathways for genes affiliated with Dfnb21 Nonsyndromic Hearing Loss and Deafness

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GO Terms for genes affiliated with Dfnb21 Nonsyndromic Hearing Loss and Deafness

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Sources for Dfnb21 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