Disease #05771 (NEDAHM (neurodevelopmental disorder with ataxia, hypotonia, and microcephaly (NEDAHM)), OMIM:618569)

Global Variome shared LOVD

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Official abbreviation	NEDAHM
Name	neurodevelopmental disorder with ataxia, hypotonia, and microcephaly (NEDAHM)
OMIM ID	618569
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CCDC23
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-06-12 17:38:55 +02:00 (CEST)
Date last edited	N/A

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