Phenotype #0000017368
| Individual ID |
00019576 |
| Associated disease |
DTDP2 |
| Phenotype details |
primary teeth severe amber color, moderate increased constriction at CEJ, moderate attrition, severe obliterated pulps, severe obliterated root canals, no thistle-tube or funnel shape of pulp chamber, mild thinner roots, no periapical radiolucencies, no shell teeth; permanent teeth mild amber color, mild increased constriction at CEJ, moderate obliterated pulps in erupted teeth, moderate obliterated pulps in unerupted teeth, moderate obliterated root canals in erupted teeth, severe thistle-tube or funnel shape of pulp chamber, mild shorter root length, mild thinner roots, no periapical radiolucencies |
| Diagnosis/Initial |
dentinogenesis imperfecta mild |
| Inheritance |
Familial, autosomal dominant |
| Diagnosis/Definite |
DTDP2 |
| 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 22:41:15 +02:00 (CEST) |
| Date last edited |
2022-11-16 12:36:58 +01:00 (CET) |
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