Disease #04356 (AI1F (amelogenesis imperfecta, type IF (AI1F)), OMIM:616270)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	AI1F
Name	amelogenesis imperfecta, type IF (AI1F)
OMIM ID	616270
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	AMBN
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 10:25:22 +02:00 (CEST)
Date last edited	2021-10-17 20:58:16 +02:00 (CEST)

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