All diseases

OMIM ID
204650
OMIM term:
AMELOGENESIS IMPERFECTA, TYPE IC; AI1C
Alternative terms:
AMELOGENESIS IMPERFECTA, LOCAL HYPOPLASTIC TYPE, AUTOSOMAL RECESSIVE
AMELOGENESIS IMPERFECTA, HYPOPLASTIC, WITH OR WITHOUT OPENBITE MALOCCLUSION, AUTOSOMAL RECESSIVE
(∗) Location:
4q13.3  
(†) Associated OMIM genes:
ENAM  
(‡) Associated MGI genes:

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