Dentin dysplasia type II

General Information (adopted from Orphanet):

Synonyms, Signs: ANOMALOUS DYSPLASIA OF DENTIN
PULPAL DYSPLASIA
DENTIN DYSPLASIA, SHIELDS TYPE II
PULP STONES
CORONAL DENTIN DYSPLASIA
DTDP2
DD-II
Number of Symptoms 9
OrphanetNr: 99791
OMIM Id: 125420
ICD-10: K00.5
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Autosomal dominant
[Orphanet]
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: Dentin dysplasia
 -Rare genetic disease
 -Rare odontologic disease

Symptom Information: Sort by abundance 

1
 (HPO:0003771) Pulp stones 6 / 7739
2
 (HPO:0011060) Dentinogenesis imperfecta limited to primary teeth 3 / 7739
3
 (OMIM) Multiple pulp stones (secondary teeth) 1 / 7739
4
 (OMIM) Thistle-shaped pulp chambers (secondary teeth) 1 / 7739
5
 (OMIM) Normal coloration (secondary teeth) 1 / 7739
6
 (HPO:0000006) Autosomal dominant inheritance 2518 / 7739
7
 (OMIM) Normal-shaped roots (primary teeth) 1 / 7739
8
 (OMIM) Amber, translucent coloration (primary teeth) 1 / 7739
9
 (OMIM) Obliteration of pulp chambers following eruption (primary teeth) 1 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: