MCID: OTS010
MIFTS: 13

Otosclerosis 7

Categories: Ear diseases, Rare diseases, Genetic diseases

Aliases & Classifications for Otosclerosis 7

MalaCards integrated aliases for Otosclerosis 7:

Name: Otosclerosis 7 57 13 73
Otsc7 57

Characteristics:

OMIM:

57
Inheritance:
autosomal dominant


HPO:

32
otosclerosis 7:
Inheritance autosomal dominant inheritance


Classifications:



External Ids:

OMIM 57 611572
MedGen 42 C1969044
UMLS 73 C1969044

Summaries for Otosclerosis 7

MalaCards based summary : Otosclerosis 7, also known as otsc7, is related to otosclerosis and otosclerosis, familial. An important gene associated with Otosclerosis 7 is OTSC7 (Otosclerosis 7). Related phenotypes are otosclerosis and hearing impairment

Description from OMIM: 611572

Related Diseases for Otosclerosis 7

Diseases in the Otosclerosis family:

Otosclerosis 1 Otosclerosis 2
Otosclerosis 3 Otosclerosis 5
Otosclerosis 4 Otosclerosis 7
Otosclerosis 8 Otosclerosis 10
Otosclerosis, Familial

Diseases related to Otosclerosis 7 via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 otosclerosis 11.5
2 otosclerosis, familial 9.9

Symptoms & Phenotypes for Otosclerosis 7

Symptoms via clinical synopsis from OMIM:

57
Head And Neck Ears:
otosclerosis
hearing loss, unilateral or bilateral, conductive or mixed conductive/sensorineural


Clinical features from OMIM:

611572

Human phenotypes related to Otosclerosis 7:

32
# Description HPO Frequency HPO Source Accession
1 otosclerosis 32 HP:0000362
2 hearing impairment 32 HP:0000365

Drugs & Therapeutics for Otosclerosis 7

Search Clinical Trials , NIH Clinical Center for Otosclerosis 7

Genetic Tests for Otosclerosis 7

Anatomical Context for Otosclerosis 7

Publications for Otosclerosis 7

Variations for Otosclerosis 7

Expression for Otosclerosis 7

Search GEO for disease gene expression data for Otosclerosis 7.

Pathways for Otosclerosis 7

GO Terms for Otosclerosis 7

Sources for Otosclerosis 7

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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