All diseases

OMIM ID
130900
OMIM term:
AMELOGENESIS IMPERFECTA, TYPE III; AI3
Alternative terms:
AMELOGENESIS IMPERFECTA, HYPOCALCIFICATION TYPE, AUTOSOMAL DOMINANT; ADHCAI
AMELOGENESIS IMPERFECTA, HYPOMINERALIZATION TYPE
(∗) Location:
8q24.3  
(†) Associated OMIM genes:
FAM83H  
(‡) Associated MGI genes:

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