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MIM:613751 - HETEROTAXY, VISCERAL, 4, AUTOSOMAL; HTX4
Xenbase Genes: acvr2b
Human Disease Resource: OMIM
MONDO:0013403 - heterotaxy, visceral, 4, autosomal |
MONDO:0018677 - visceral heterotaxy |
DOID:0050545 - visceral heterotaxy |
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MONDO:0013403 - heterotaxy, visceral, 4, autosomal |
MONDO:0018677 - visceral heterotaxy |
DOID:0050545 - visceral heterotaxy |