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Rare Disease
Deafness, Autosomal Recessive 88 (DFNB88)
Alias:
Dfnb88
Autosomal Recessive Nonsyndromic Deafness 88
Autosomal Recessive Nonsyndromic Hearing Loss 88
Deafness, Autosomal Recessive, Type 88
Deafness, Autosomal Recessive, 88
Autosomal Recessive Deafness 88
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Deafness, Autosomal Recessive 88, is also known as dfnb88. An important gene associated with Deafness, Autosomal Recessive 88 is ELMOD3 (ELMO Domain Containing 3). Related phenotype is mixed hearing impairment.
Related ID:
MALACARDS:DFN243
OMIM:615429
MESH:D046089
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
--
5
15
1
DFN243
Medical Symptom
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Categorization
Description
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HPO Source Accession
No data available
Gene & Mutation
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Name
CAS Number
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No data available
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Category
Name
MGI
Related Gene
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Publications
No data available
References Literature
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IF
No Data Found!
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