Disease #00039 (GRACILE (GRACILE syndrome), OMIM:603358)

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Official abbreviation	GRACILE
Name	GRACILE syndrome
OMIM ID	603358
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	BCS1L
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-08-30 16:27:59 +02:00 (CEST)
Date last edited	N/A