Disease #00053 (RAPADILINO syndrome, OMIM:266280)

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