Phenotype #0000237152

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00312023
Associated disease	neuropathy, optic
Phenotype details	Reduced visual acuity (HP:0007663); Optic atrophy (HP:0000648); Dyschromatopsia (HP:0007641); Global developmental delay (HP:0001263)
Diagnosis/Initial	-
Diagnosis/Definite	-
Inheritance	Isolated (sporadic)
Age/Examination	07y (7 years)
Age/Diagnosis	-
Age/Onset	?
Phenotype/Onset	-
Protein	-
Owner name	Benjamin Billiet
Database submission license	No license selected
Created by	Benjamin Billiet
Date created	2020-09-30 10:49:08 +02:00 (CEST)
Date last edited	2021-05-05 16:34:12 +02:00 (CEST)

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