Details of Disease

General Information of Disease (ID: DISE4R1W)

Disease Name Dentin dysplasia type II
Synonyms
dentin dysplasia, Shields type 2; dentin dyspalsia, Shields type 2; anomalous dysplasia of dentin; dentin dysplasia, type II; Dtdp2; dentin dysplasia, coronal; coronal dentin dysplasia; pulpal dysplasia; dentin dysplasia, type 2; pulp stones; DD-II; DTDP2
Definition Dentin dysplasia type II (DD-II) is a rare mild form of dentin dysplasia (DD) characterized by normal tooth roots but abnormal primary dentition.
Disease Hierarchy
DISYKSRF: Genetic disease
DISCGIX8: Dentin dysplasia
DISE4R1W: Dentin dysplasia type II
Disease Identifiers
MONDO ID
MONDO_0007437
MESH ID
D003784
UMLS CUI
C1527284
MedGen ID
315928
HPO ID
HP:0003771
Orphanet ID
99791
SNOMED CT ID
57602001

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
DSPP OT1TYNDN Supportive Autosomal dominant [1]
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References

1 Clinical Practice Guidelines for Rare Diseases: The Orphanet Database. PLoS One. 2017 Jan 18;12(1):e0170365. doi: 10.1371/journal.pone.0170365. eCollection 2017.