All diseases

OMIM ID
104500
OMIM term:
AMELOGENESIS IMPERFECTA, TYPE IB; AI1B
Alternative terms:
AMELOGENESIS IMPERFECTA, HYPOPLASTIC LOCAL, AUTOSOMAL DOMINANT
AIH2
ENAMEL HYPOPLASIA, HEREDITARY LOCALIZED
(∗) Location:
4q13.3  
(†) Associated OMIM genes:
ENAM  
(‡) Associated MGI genes:
Enam  

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