Chromosome Xq21 Deletion Syndrome

Alias:
Choroideremia, Deafness, and Mental Retardation
Xq21 Deletion Syndrome
Ayazi Syndrome
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Chromosome Xq21 Deletion Syndrome, also known as choroideremia, deafness, and mental retardation, is related to deafness, x-linked 2 and choroideremia. An important gene associated with Chromosome Xq21 Deletion Syndrome is DELXQ21 (Choroideremia, Deafness, And Mental Retardation). Affiliated tissues include retina and bone, and related phenotypes are intellectual disability and hearing impairment

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
XL
XLD
Newborn
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Medical Symptom

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Gene & Mutation

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Related Drugs

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Disease Model

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References Literature

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