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At a Glance
Usher syndrome type 2c, GPR98/PDZD digenic; Deafness, X-linked 6; Deafness, autosomal dominant 36 more...
ABHD12 (20p11.21); ADGRV1 (5q14.3); CDH23 (10q22.1); CIB2 (15q25.1); CLRN1 (3q25.1) more...
Conditions Help
Total conditions: 19
Condition/Phenotype Identifier
Methodology
Total methods: 0
Method Category Help
Test method Help
Instrument *
* Instrument: Not provided
Technical Information
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Additional Information

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