Phenotypes for disease #00444 (DTDP2 (dysplasia, dentin, type 2 (DTDP-2)), OMIM:125420)

8 entries on 1 page. Showing entries 1 - 8.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000017362 primary teeth severe amber color, no increased constriction at CEJ, no attrition, moderate obliterated pulps, moderate obliterated root canals, severe thistle-tube or funnel shape of pulp chamber, no shorter root length, no thinner roots, no periapical radiolucencies, no shell teeth; permanent teeth no amber color, no increased constriction at CEJ, no attrition, no obliterated pulps in unerupted teeth, dentinogenesis imperfecta mild DTDP2 Familial, autosomal dominant - - - - - Muriel de La Dure-Molla 00019570
0000017363 primary teeth severe amber color, moderate increased constriction at CEJ, moderate attrition, moderate obliterated pulps, moderate obliterated root canals, mild thistle-tube or funnel shape of pulp chamber, mild shorter root length, moderate thinner roots, no periapical radiolucencies, no shell teeth; permanent teeth mild amber color, mild increased constriction at CEJ, no attrition, mild obliterated pulps in erupted teeth, no obliterated pulps in unerupted teeth, moderate obliterated root canals in erupted teeth, no obliterated root canals in unerupted teeth, moderate thistle-tube or funnel shape of pulp chamber, no shorter root length, mild thinner roots, no periapical radiolucencies dentinogenesis imperfecta mild DTDP2 Familial, autosomal dominant - - - - - Muriel de La Dure-Molla 00019571
0000017364 dentinogenesis imperfecta mild - - Familial, autosomal dominant - - - - - Muriel de La Dure-Molla 00019572
0000017365 dentinogenesis imperfecta mild - - Familial, autosomal dominant - - - - - Muriel de La Dure-Molla 00019573
0000017366 permanent teeth no amber color, no increased constriction at CEJ, mild attrition, moderate obliterated pulps in erupted teeth, moderate obliterated root canals in erupted teeth, severe thistle-tube or funnel shape of pulp chamber, no shorter root length, moderate thinner roots, no periapical radiolucencies dentinogenesis imperfecta mild/moderate DTDP2 Familial, autosomal dominant - - - - - Muriel de La Dure-Molla 00019574
0000017367 dentinogenesis imperfecta mild/moderate - - Familial, autosomal dominant - - - - - Muriel de La Dure-Molla 00019575
0000017368 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 dentinogenesis imperfecta mild DTDP2 Familial, autosomal dominant - - - - - Muriel de La Dure-Molla 00019576
0000017375 dentinogenesis imperfecta mild/moderate - - Familial, autosomal dominant - - - - - Muriel de La Dure-Molla 00019584
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.