Phenotype #0000302455

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Individual ID	00410351
Associated disease	HARP
Phenotype details	-
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	pantothenate kinase associated neurodegeneration
Age/Examination	-
Age/Diagnosis	02y
Age/Onset	01y
Phenotype/Onset	developmental delay
Protein	-
Owner name	LOVD
Database submission license
Created by	Anna Tracewska
Date created	2022-05-24 14:37:58 +02:00 (CEST)
Date last edited	2022-05-24 14:58:37 +02:00 (CEST)

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