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MIM:614779 - HETEROTAXY, VISCERAL, 6, AUTOSOMAL; HTX6
Xenbase Genes: cfap53
Human Disease Resource: OMIM
MONDO:0013887 - heterotaxy, visceral, 6, autosomal |
MONDO:0018677 - visceral heterotaxy |
DOID:0050545 - visceral heterotaxy |
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MONDO:0013887 - heterotaxy, visceral, 6, autosomal |
MONDO:0018677 - visceral heterotaxy |
DOID:0050545 - visceral heterotaxy |