Disease #04515 (LCDD (lacrimal duct defect? (LCDD)), OMIM:149700)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curators: Guiomar Perez de Nanclares, Francesca Marta Elli, and Giovanna Mantovani

Official abbreviation	LCDD
Name	lacrimal duct defect? (LCDD)
OMIM ID	149700
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	IGSF3
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 10:25:22 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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