Dentin Dysplasia, Type I (DTDP1)

Alias:
Radicular Dentin Dysplasia
Dentin Dysplasia Type I
Dtdp1
Rootless Teeth
Dd-I
Dentin Dysplasia, Type I, with Extreme Microdontia and Misshapen Teeth
Dentin Dysplasia 1, with Extreme Microdontia and Misshapen Teeth
Dentin Dysplasia, Type I, with Microdontia and Misshapen Teeth
Dentin Dysplasia Type 1 with Microdontia and Shape Anomalies
Atypical Dentin Dysplasia Due to Smoc2 Deficiency
Dentin Dysplasia, Shields Type I
Dentin Dysplasia Shields Type I
Dentin Dysplasia, Radicular
Dysplasia, Dentin, Type I
Dentin Dysplasia 1
Dtdp1-Mmt
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Dentin Dysplasia, Type I, also known as radicular dentin dysplasia, is related to dentin dysplasia and tooth agenesis. An important gene associated with Dentin Dysplasia, Type I is SMOC2 (SPARC Related Modular Calcium Binding 2). Affiliated tissues include bone and brain, and related phenotypes are microdontia and taurodontia
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
AD
Newborn
1-9/100000
4
26
12

Medical Symptom

#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

#
Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
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