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GENATLAS PHENOTYPE |
last update : 01-09-2021 |
Symbol | AI1F |
Location | 4q13.3 |
Name | amelogenesis imperfecta, type IF |
Corresponding gene | AMBN |
Main clinical features |
|
Genetic determination | autosomal recessive |
Function/system disorder | digestive tract/liver and annex |
Type | disease |
Remark(s) |