Disease #04527 (AI-1H (amelogenesis imperfecta, type IH (AI-1H)), OMIM:616221)

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Official abbreviation	AI-1H
Name	amelogenesis imperfecta, type IH (AI-1H)
OMIM ID	616221
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ITGB6
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 10:25:22 +02:00 (CEST)
Date last edited	N/A