Branchiootic Syndrome 3 (BOS3)

Branchiootic Syndrome 3(来自ICD-11)

别称:

Bo Syndrome 3

Bos3

Branchiootic Syndrome, Type 3

Branchio-Otic Dysplasia 3

Branchio-Otic Syndrome 3

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Branchiootic Syndrome 3, also known as bo syndrome 3, is related to deafness, unilateral and branchiootorenal syndrome 1. An important gene associated with Branchiootic Syndrome 3 is SIX1 (SIX Homeobox 1). Affiliated tissues include skin and lung, and related phenotypes are sensorineural hearing impairment and preauricular skin tag

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