Disease #05529 (PRPTS (Pierpont syndrome (PRPTS)), OMIM:602342)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	PRPTS
Name	Pierpont syndrome (PRPTS)
OMIM ID	602342
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TBL1XR1
Associated tissues	-
Disease features	autosomal dominant
Remarks	-
Date created	2018-12-02 17:46:12 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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