Phenotype #0000052835

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00073166
Associated disease	ALMS
Phenotype details	Visual loss (HP:0000572), Photophobia (HP:0000613), Pendular nystagmus (HP:0012043),
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Pieter Klap
Database submission license	No license selected
Created by	Pieter Klap
Date created	2016-06-09 11:16:22 +02:00 (CEST)
Date last edited	2016-10-11 12:31:54 +02:00 (CEST)

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