Disease #06946 (NEDMISB (neurodevelopmental disorder with microcephaly, seizures, and brain atrophy), OMIM:619076)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	NEDMISB
Name	neurodevelopmental disorder with microcephaly, seizures, and brain atrophy
OMIM ID	619076
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	EXOC8
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-07-18 13:36:33 +02:00 (CEST)
Date last edited	N/A

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