Disease #00204 (WRN (WERNER SYNDROME), OMIM:277700)

MVZ für Humangenetik Regensburg

LOVD v.3.0 Build 30 [ Current LOVD status ]
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Official abbreviation	WRN
Name	WERNER SYNDROME
OMIM ID	277700
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	WRN
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-06-03 15:25:33 +00:00 (UTC)
Date last edited	N/A