Disease #04553 (AI1A (amelogenesis imperfecta, type IA (AI1A)), OMIM:104530)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	AI1A
Name	amelogenesis imperfecta, type IA (AI1A)
OMIM ID	104530
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	LAMB3
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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