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MIM:606713 - VAN DER WOUDE SYNDROME 2; VWS2
Xenbase Genes: grhl3
Human Disease Resource: OMIM
MONDO:0011712 - van der Woude syndrome 2 |
MONDO:0019508 - van der Woude syndrome |
DOID:0060239 - Van der Woude syndrome |
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MONDO:0011712 - van der Woude syndrome 2 |
MONDO:0019508 - van der Woude syndrome |
DOID:0060239 - Van der Woude syndrome |