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MIM:608572 - BURN-MCKEOWN SYNDROME; BMKS
Xenbase Genes: txnl4a
Human Disease Resource: MIM
MONDO:0012064 - choanal atresia-hearing loss-cardiac defects-craniofacial dysmorphism syndrome |
DOID:0080695 - Burn-McKeown syndrome |
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MONDO:0012064 - choanal atresia-hearing loss-cardiac defects-craniofacial dysmorphism syndrome |
DOID:0080695 - Burn-McKeown syndrome |