Disease #03511 (DKCA-3 (dyskeratosis congenita, autosomal dominant, type 3 (DKCA-3)), OMIM:613990)

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Official abbreviation	DKCA-3
Name	dyskeratosis congenita, autosomal dominant, type 3 (DKCA-3)
OMIM ID	613990
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TINF2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A