Disease #02211 (AI1E (amelogenesis imperfecta, type IE (AI1E)), OMIM:301200)

Official abbreviation AI1E
Name amelogenesis imperfecta, type IE (AI1E)
OMIM ID 301200
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene AMELX
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00479897 - - - F no Brazil - - - - - AI1E hypoplastic amelogenesis imperfecta, with vertical grooves located in the incisal and middle thirds of the crown - AMELX 1 1 Juliana Mazzeu
00479898 - - - M no Brazil - - - - - AI1E Hypoplastic amelogenesis imperfecta - AMELX 1 1 Juliana Mazzeu
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