Disease #00642 (LPRD-3 (LEOPARD syndrome, type 3 (LPRD-3)), OMIM:613707)

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Official abbreviation	LPRD-3
Name	LEOPARD syndrome, type 3 (LPRD-3)
OMIM ID	613707
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	BRAF
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A