Disease #05673 (FASPS3 (sleep phase syndrome, advanced, familial, type 3 (FASPS3)), OMIM:616882)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

Official abbreviation	FASPS3
Name	sleep phase syndrome, advanced, familial, type 3 (FASPS3)
OMIM ID	616882
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PER3
Associated tissues	-
Disease features	-
Remarks	-
Date created	2019-11-04 08:54:30 +01:00 (CET)
Date last edited	N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.