View disease #00009

Official abbreviation AI unclassified
Name Amelogenesis imperfecta - not classified
OMIM ID -
Individuals reported having this disease 12
Phenotype entries for this disease 12
Associated with 0 genes -


Individuals

12 entries on 1 page. Showing entries 1 - 12.
Legend  

AscendingIndividual ID     

Reference     

Remarks     

Disease     

Genes screened

Variants     

Panel size     

Owner     
00000134 McGrath et al. 1996 - AI unclassified COL17A1 1 1 Claire Smith
00000135 Tasanen et al. 2000 German origin AI unclassified COL17A1 1 1 Claire Smith
00000136 Vaisanen et al. 2005 - AI unclassified COL17A1 1 1 Claire Smith
00000137 Väisänen et al. 2005 Turkish origin AI unclassified COL17A1 1 1 Claire Smith
00000138 Väisänen et al. 2005 German origin AI unclassified COL17A1 1 1 Claire Smith
00000159 Gostyńska et al. 2016 Dutch origin; father of individual with JEB. AI unclassified LAMA3 1 1 Henny Lemmink
00000160 Gostyńska et al. 2016 Dutch origin; mother of individual with JEB AI unclassified LAMA3 1 1 Henny Lemmink
00000164 Ansar et al. 2016 Pakistani origin; syndromic disease. 3 affected individuals, plus 4 unaffected individuals used for segregation. AI unclassified ITGB6 1 1 Claire Smith
00000187 Mayer et al. 2009 Austrian study. AI unclassified DLX3 1 1 Claire Smith
00000191 Wright et al. 2008 US study AI unclassified DLX3 1 1 Claire Smith
00000193 Price et al. 1998 US origin: North Carolina; 6 families identified AI unclassified DLX3 1 6 Claire Smith
00000194 Price et al. 1998 US origin: Virginia AI unclassified DLX3 1 1 Claire Smith
Legend