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Last updated in GTR:
At a Glance
Autosomal recessive nonsyndromic hearing loss 63; Autosomal dominant Alport syndrome; Autosomal dominant nonsyndromic hearing loss 1; ...
ACTG1 (17q25.3), ADGRV1 (5q14.3), ATP6V1B1 (2p13.3), BSND (1p32.3), CACNA1D (3p21.1), ...
Conditions Help
Total conditions: 108
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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