Disease #07152 (HTX14 (heterotaxy, visceral, type 14), OMIM:621080)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Official abbreviation	HTX14
Name	heterotaxy, visceral, type 14
OMIM ID	621080
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	C1orf127
Associated tissues	-
Disease features	-
Remarks	-
Date created	2025-02-09 09:53:46 +01:00 (CET)
Date last edited	N/A

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