Disease #05366 (NDAGSCW (neurodevelopmental disorder with ataxic gait, absent speech, decreased cortical white matter (NDAGSCW)), OMIM:617807)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	NDAGSCW
Name	neurodevelopmental disorder with ataxic gait, absent speech, decreased cortical white matter (NDAGSCW)
OMIM ID	617807
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	RAB11B
Associated tissues	-
Disease features	-
Remarks	-
Date created	2017-12-29 15:08:18 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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