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 57

Characteristics:

OMIM:

57
Inheritance:
autosomal dominant


HPO:

32
deafness, mid-tone neural:
Onset and clinical course childhood onset
Inheritance autosomal dominant inheritance


Classifications:



External Ids:

OMIM 57 124700
MedGen 42 C1852283
SNOMED-CT via HPO 69 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

Symptoms via clinical synopsis from OMIM:

57
Misc:
onset in childhood

Ears:
neural hearing loss
progressive hearing loss
midfrequency hearing loss


Clinical features from OMIM:

124700

Human phenotypes related to Deafness, Mid-Tone Neural:

32
# Description HPO Frequency HPO Source Accession
1 sensorineural hearing impairment 32 HP:0000407
2 progressive hearing impairment 32 HP:0001730

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 ExPASy
19 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 LOVD
42 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
54 NINDS
55 Novoseek
57 OMIM
58 OMIM via Orphanet
62 PubMed
64 QIAGEN
69 SNOMED-CT via HPO
70 SNOMED-CT via Orphanet
71 TGDB
72 Tocris
73 UMLS
74 UMLS via Orphanet
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