Disease #00166 (NBSLD (Nijmegen breakage syndrome-like disorder (NBSLD)), OMIM:613078)

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Official abbreviation	NBSLD
Name	Nijmegen breakage syndrome-like disorder (NBSLD)
OMIM ID	613078
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	RAD50
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-07-21 20:24:30 +02:00 (CEST)
Date last edited	N/A