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MIM:611383 - USHER SYNDROME, TYPE IID; USH2D
Xenbase Genes: whrn
Human Disease Resource: OMIM
MONDO:0012662 - Usher syndrome type 2D |
MONDO:0016484 - Usher syndrome type 2 |
MONDO:0019501 - Usher syndrome |
DOID:0110840 - Usher syndrome type 2D |
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MONDO:0012662 - Usher syndrome type 2D |
MONDO:0016484 - Usher syndrome type 2 |
MONDO:0019501 - Usher syndrome |
DOID:0110840 - Usher syndrome type 2D |