Disease #05614 (DYTOABG (dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities (DYTOABG)), OMIM:617282)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	DYTOABG
Name	dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities (DYTOABG)
OMIM ID	617282
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MECR
Associated tissues	-
Disease features	autosomal recessive
Remarks	-
Date created	2019-06-19 19:05:46 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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