Disease #00046 (lactase def. (lactase deficiency, congenital), OMIM:223000)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	lactase def.
Name	lactase deficiency, congenital
OMIM ID	223000
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	LCT
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-08-30 17:31:00 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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