Phenotype #0000302159

Global Variome shared LOVD

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

Individual ID	00410050
Associated disease	OPMD
Phenotype details	clinically definite oculopharyngeal muscular dystrophy, late onset; no retinal dystrophy
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	oculopharyngeal muscular dystrophy
Age/Examination	83y (83 years)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	LOVD
Database submission license
Created by	Anna Tracewska
Date created	2022-05-18 12:34:52 +02:00 (CEST)
Date last edited	N/A

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