Disease #06884 (SMDP (dysplasia, spondylometaphyseal, Pagnamenta type), OMIM:619638)

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	SMDP
Name	dysplasia, spondylometaphyseal, Pagnamenta type
OMIM ID	619638
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 17:31:03 +01:00 (CET)
Date last edited	N/A

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