Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness (EDMMD)

Alias:
Multiple Epiphyseal Dysplasia, Beighton Type
Edmmd
Epiphyseal Dysplasia, Multiple, with Myopia and Deafness
Multiple Epiphyseal Dysplasia with Myopia and Deafness
Multiple Epiphyseal Dysplasia-Myopia-Deafness Syndrome
Multiple Epiphyseal Dysplasia with Myopia and Conductive Deafness
Multiple Epiphyseal Dysplasia-Myopia-Hearing Loss Syndrome
Dysplasia, Epiphyseal, Multiple, with Myopia and Deafness
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness, also known as multiple epiphyseal dysplasia, beighton type, is related to tracheal disease and spondyloarthropathy. An important gene associated with Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness is COL2A1 (Collagen Type II Alpha 1 Chain), and among its related pathways/superpathways is C-MYB transcription factor network. Affiliated tissues include bone and eye, and related phenotypes are biconcave vertebral bodies and multiple epiphyseal dysplasia
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Newborn
<1/1000000
5
57
2

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

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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
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IF
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