Disease #05983 (TPFS (Turnpenny-Fry syndrome (TPFS)), OMIM:618371)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	TPFS
Name	Turnpenny-Fry syndrome (TPFS)
OMIM ID	618371
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PCGF2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-10-28 11:14:55 +02:00 (CEST)
Date last edited	N/A

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