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MIM:605376 - HETEROTAXY, VISCERAL, 2, AUTOSOMAL; HTX2
Xenbase Genes:
Human Disease Resource: OMIM
MONDO:0011546 - heterotaxy, visceral, 2, autosomal |
MONDO:0018677 - visceral heterotaxy |
DOID:0050545 - visceral heterotaxy |
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MONDO:0011546 - heterotaxy, visceral, 2, autosomal |
MONDO:0018677 - visceral heterotaxy |
DOID:0050545 - visceral heterotaxy |