Disease #07074 (ARCND2B (auriculocondylar syndrome, type 2B), OMIM:620458)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	ARCND2B
Name	auriculocondylar syndrome, type 2B
OMIM ID	620458
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PLCB4
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-03-19 12:52:51 +01:00 (CET)
Date last edited	N/A

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