Disease #06661 (NADGP (Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset), OMIM:617145)

Global Variome shared LOVD

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Official abbreviation	NADGP
Name	Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset
OMIM ID	617145
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SQSTM1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	N/A

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