Disease #00442 (DGI3 (dentinogenesis imperfecta, Shields type III (DGI-3)), OMIM:125500)

Official abbreviation DGI3
Name dentinogenesis imperfecta, Shields type III (DGI-3)
OMIM ID 125500
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene DSPP
Associated tissues -
Disease features -
Remarks -
Date created 2014-07-09 12:54:35 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00019589 - PubMed: Dong 2005 5-generation family, 13 affecteds (7F, 6M) - no United States - - - - - DGI3 dentinogenesis imperfecta severe DSPP DSPP 2 13 Muriel de La Dure-Molla
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