All diseases

OMIM ID
301200
OMIM term:
AMELOGENESIS IMPERFECTA, TYPE IE; AI1E
Alternative terms:
AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 1
AMELOGENESIS IMPERFECTA, X-LINKED 1; AIH1
ENAMEL HYPOPLASIA, X-LINKED AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, WITH SNOW-CAPPED TEETH, INCLUDED
(∗) Location:
Xp22.2  
(†) Associated OMIM genes:
AMELX  
(‡) Associated MGI genes:
Amelx  

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