Phenotype #0000017372
| Individual ID |
00019581 |
| Associated disease |
DGI1 |
| Phenotype details |
primary teeth severe amber color, mild increased constriction at CEJ, no attrition, severe obliterated pulps, no periapical radiolucencies, ; permanent teeth severe amber color, mild increased constriction at CEJ, no attrition, severe obliterated pulps in erupted teeth, severe obliterated pulps in unerupted teeth, severe obliterated root canals in erupted teeth, severe obliterated root canals in unerupted teeth, no thistle-tube or funnel shape of pulp chamber, mild shorter root length, mild thinner roots, no periapical radiolucencies |
| Diagnosis/Initial |
dentinogenesis imperfecta moderate |
| Inheritance |
Familial, autosomal dominant |
| Diagnosis/Definite |
DGI1 |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Muriel de La Dure-Molla |
| Database submission license |
No license selected |
| Created by |
Muriel de La Dure-Molla |
| Date created |
2014-07-29 23:03:46 +02:00 (CEST) |
| Date last edited |
2022-11-16 12:43:00 +01:00 (CET) |
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