Disease #00053 (RAPADILINO (RAPADILINO syndrome), OMIM:266280)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Cynthia Silveira

Official abbreviation	RAPADILINO
Name	RAPADILINO syndrome
OMIM ID	266280
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	1
Associated with 1 gene	RECQL4
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-08-31 10:07:24 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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