Phenotype #0000043005

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00056386
Associated disease	PRLTS3;DFNB81
Phenotype details	see paper; ..., Perrault syndrome (PRTLS)
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Leigh Demain
Database submission license	No license selected
Created by	Johan den Dunnen
Date created	2015-12-18 07:21:34 +01:00 (CET)
Date last edited	2016-11-10 12:25:08 +01:00 (CET)

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