MCID: DFN339
MIFTS: 7

Deafness, Mid-Tone Neural

Categories: Ear diseases

Aliases & Classifications for Deafness, Mid-Tone Neural

MalaCards integrated aliases for Deafness, Mid-Tone Neural:

Name: Deafness, Mid-Tone Neural 58

Characteristics:

OMIM:

58
Inheritance:
autosomal dominant


HPO:

33
deafness, mid-tone neural:
Onset and clinical course childhood onset
Inheritance autosomal dominant inheritance


Classifications:



External Ids:

OMIM 58 124700
MedGen 43 C1852283
SNOMED-CT via HPO 70 263681008 60700002

Summaries for Deafness, Mid-Tone Neural

MalaCards based summary : Deafness, Mid-Tone Neural Related phenotypes are sensorineural hearing impairment and progressive hearing impairment

Description from OMIM: 124700

Related Diseases for Deafness, Mid-Tone Neural

Symptoms & Phenotypes for Deafness, Mid-Tone Neural

Human phenotypes related to Deafness, Mid-Tone Neural:

33
# Description HPO Frequency HPO Source Accession
1 sensorineural hearing impairment 33 HP:0000407
2 progressive hearing impairment 33 HP:0001730

Symptoms via clinical synopsis from OMIM:

58
Misc:
onset in childhood

Ears:
neural hearing loss
progressive hearing loss
midfrequency hearing loss

Clinical features from OMIM:

124700

Drugs & Therapeutics for Deafness, Mid-Tone Neural

Search Clinical Trials , NIH Clinical Center for Deafness, Mid-Tone Neural

Genetic Tests for Deafness, Mid-Tone Neural

Anatomical Context for Deafness, Mid-Tone Neural

Publications for Deafness, Mid-Tone Neural

Variations for Deafness, Mid-Tone Neural

Expression for Deafness, Mid-Tone Neural

Search GEO for disease gene expression data for Deafness, Mid-Tone Neural.

Pathways for Deafness, Mid-Tone Neural

GO Terms for Deafness, Mid-Tone Neural

Sources for Deafness, Mid-Tone Neural

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
20 FMA
29 GO
30 GTR
31 HGMD
32 HMDB
33 HPO
34 ICD10
35 ICD10 via Orphanet
36 ICD9CM
37 IUPHAR
38 KEGG
39 LifeMap
41 LOVD
43 MedGen
45 MeSH
46 MESH via Orphanet
47 MGI
50 NCI
51 NCIt
52 NDF-RT
55 NINDS
56 Novoseek
58 OMIM
59 OMIM via Orphanet
63 PubMed
65 QIAGEN
70 SNOMED-CT via HPO
71 SNOMED-CT via Orphanet
72 TGDB
73 Tocris
74 UMLS
75 UMLS via Orphanet
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