Deafness, Autosomal Recessive 120 (DFNB120)

Alias:
Dfnb120
Hearing Loss, Autosomal Recessive 120
Deafness, Autosomal Recessive, 120
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Deafness, Autosomal Recessive 120, is also known as dfnb120. An important gene associated with Deafness, Autosomal Recessive 120 is MINAR2 (Membrane Integral NOTCH2 Associated Receptor 2). Affiliated tissues include brain, and related phenotype is sensorineural hearing impairment.
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
--
2
10
1

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
Year
IF
No Data Found!
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