Orphanet Rare Disease Ontology

Last uploaded: December 4, 2024

Id	http://www.orpha.net/ORDO/Orphanet_1653 http://www.orpha.net/ORDO/Orphanet_1653
Preferred Name	Dentin dysplasia
Definitions	Dentin dysplasia (DD) is a rare disorder belonging to the group of hereditary dentin defects (see this term) and is characterized by abnormal dentin structure and root development resulting in abnormal tooth development. It encompasses two subtypes: DD type I and DD type II (see these terms).
Synonyms	DD
Type	http://www.w3.org/2002/07/owl#Class

definition_citation	Orphanet
definition	Dentin dysplasia (DD) is a rare disorder belonging to the group of hereditary dentin defects (see this term) and is characterized by abnormal dentin structure and root development resulting in abnormal tooth development. It encompasses two subtypes: DD type I and DD type II (see these terms).
label	Dentin dysplasia
prefLabel	Dentin dysplasia
hasDbXref	MeSH:D003805 OMIM:125400 ICD-10:K00.5 ICD-11:LA30.7 UMLS:C0011430 OMIM:125420 See more See less
notation	ORPHA:1653
alternative_term	DD
present_in	Worldwide AND has_point_prevalence_range : Unknown
part_of	http://www.orpha.net/ORDO/Orphanet_167759
prefixIRI	ORDO:Orphanet_1653
expertlink	https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=1653
subClassOf	http://www.orpha.net/ORDO/Orphanet_377788 http://www.orpha.net/ORDO/Orphanet_557493
type	http://www.w3.org/2002/07/owl#Class
has_inheritance	Autosomal dominant
has_age_of_onset	All ages
treeView	http://www.orpha.net/ORDO/Orphanet_167759

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