Phenotype #0000155191

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00207418
Associated disease	LS
Inheritance	Familial, autosomal recessive
Diagnosis/Initial	-
Age/Examination	-
Diagnosis/Definite	-
Age/Diagnosis	-
Age/Onset	00y04m
Phenotype/Onset	-
Phenotype details	Leigh-like, profound global developmental delay(HP:0001263), hypotonia and seizures (HP:0001250)
Protein	-
Owner name	Sze Chern Lim
Database submission license	No license selected
Created by	Sze Chern Lim
Date created	2018-11-22 07:24:48 +01:00 (CET)
Date last edited	2018-11-22 09:24:21 +01:00 (CET)

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