Disease #07282 (RAMELN (Ramond-Elliott neurodevelopmental syndrome), OMIM:621421)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Coline van Moorsel

Official abbreviation	RAMELN
Name	Ramond-Elliott neurodevelopmental syndrome
OMIM ID	621421
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TRA2B
Associated tissues	-
Disease features	-
Remarks	-
Date created	2026-09-10 10:55:23 +02:00 (CEST)
Date last edited	N/A

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