Brachydactyly, Type A3 (BDA3)

Alias:
Brachydactyly Type A3
Brachydactyly-Clinodactyly
Brachymesophalangy V
Bda3
Brachydactyly Clinodactyly
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Brachydactyly, Type A3, also known as brachydactyly type a3, is related to neurodevelopmental, jaw, eye, and digital syndrome and robin sequence with distinctive facial appearance and brachydactyly. An important gene associated with Brachydactyly, Type A3 is HOXD13 (Homeobox D13), and among its related pathways/superpathways is COPI-independent Golgi-to-ER retrograde traffic. Affiliated tissues include heart and bone, and related phenotypes are clinodactyly of the 5th finger and cone-shaped epiphysis
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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9
48
4

Medical Symptom

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Description
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Gene & Mutation

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Disease Model

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MGI
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Publications
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References Literature

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