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MIM:606325 - HETEROTAXY, VISCERAL, 3, AUTOSOMAL; HTX3
Xenbase Genes:
Human Disease Resource: MIM
MONDO:0011659 - heterotaxy, visceral, 3, autosomal |
MONDO:0018677 - visceral heterotaxy |
DOID:0050545 - visceral heterotaxy |
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MONDO:0011659 - heterotaxy, visceral, 3, autosomal |
MONDO:0018677 - visceral heterotaxy |
DOID:0050545 - visceral heterotaxy |