- OMIM ID
-
301201
- OMIM term:
- AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 2
- Alternative terms:
-
AMELOGENESIS IMPERFECTA 3, HYPOPLASTIC TYPE, FORMERLY; AIH3, FORMERLY
ENAMEL HYPOPLASIA, X-LINKED
- (∗) Location:
- Xq22-q28
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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