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MIM:607842 - AURAL ATRESIA, CONGENITAL; CAA
Xenbase Genes: tshz1
Human Disease Resource: MIM
| MONDO:0011921 - connecting stalk blood islands |
| MONDO:0015385 - obsolete external auditory canal aplasia/hypoplasia |
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| MONDO:0011921 - connecting stalk blood islands |
| MONDO:0015385 - obsolete external auditory canal aplasia/hypoplasia |