Disease #05733 (HTX7 (heterotaxy, visceral, autosomal, type 7 (HTX7)))

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	HTX7
Name	heterotaxy, visceral, autosomal, type 7 (HTX7)
OMIM ID	-
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MMP21
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-04-27 09:48:09 +02:00 (CEST)
Date last edited	N/A

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