Disease #06883 (AMD4 (dysplasia, acromesomelic, type 4), OMIM:619636)

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	AMD4
Name	dysplasia, acromesomelic, type 4
OMIM ID	619636
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PRKG2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-16 17:29:30 +01:00 (CET)
Date last edited	N/A

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