Disease Browser
Parent Node: Tooth Abnormalities (D014071) ..Starting node .. Dentin Dysplasia (D003805) Child Nodes:
........Dentin dysplasia sclerotic bones (C538213) ........Dentin dysplasia, type 1 (C538215) ........DENTIN DYSPLASIA, TYPE II (OMIM:125420) Sister Nodes: ..Ackerman syndrome (C538170) ..Anodontia (D000848) 29 ..AREDYLD Syndrome (C537427) ..Blepharo-cheilo-dontic syndrome (C536188) ..Book Syndrome (C562993) ..Carabelli Anomaly of Maxillary Molar Teeth (C566175) ..Cleidocranial Dysplasia, Forme Fruste, Dental Anomalies Only (C563974) ..CODAS syndrome (C536434) ..Deafness with Labyrinthine Aplasia Microtia and Microdontia (LAMM) (C548011) ..Deafness, Congenital, and Onychodystrophy, Autosomal Dominant (C567274) ..Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia (C565195) ..Dens in Dente (D003719) 1 ..Dental Enamel Hypoplasia (D003744) 29 ..Dentin Dysplasia (D003805) 3 ..Dentinogenesis Imperfecta (D003811) 7 ..Dermoodontodysplasia (C565103) ..Diastema, Dental Medial (C565098) ..Euhidrotic ectodermal dysplasia (C535763) ..Facial Dysmorphism, Selective Tooth Agenesis, and Choroid Calcification (C567039) ..Faciocardiomelic Dysplasia, Lethal (C565578) ..Fused Teeth (D005671) ..Grubben de Cock Borghgraef syndrome (C537621) ..Hypoglossia-Hypodactylia (C566308) ..Iridogoniodysgenesis, dominant type (C535536) ..Kallmann Syndrome 2 with Selective Tooth Agenesis (C566948) ..KBG syndrome (C537015) ..Lacrimoauriculodentodigital syndrome (C538132) ..Larsen syndrome, dominant type (C537873) ..Nance-Horan syndrome (C538336) ..Oculodentodigital Dysplasia (C563160) ..Oculodentodigital Dysplasia, Autosomal Recessive (C567605) ..Oculotrichodysplasia (C564934) ..Odontodysplasia (D018126) 3 ..Odontomicronychial dysplasia (C537741) ..Odontotrichoungual-Digital-Palmar Syndrome (C566598) ..Oroacral Syndrome, Verloes-Koulischer Type (C566374) ..Otodental Dysplasia (C563482) ..Polydactyly, Postaxial, with Dental and Vertebral Anomalies (C564880) ..Rodrigues blindness (C535865) ..Spondyloepimetaphyseal Dysplasia With Abnormal Dentition (C566644) ..Taurodontism (C536946) ..Taurodontism, microdontia, and dens invaginatus (C536947) ..Teeth noneruption of with maxillary hypoplasia and genu valgum (C536952) ..Teeth, Odd Shapes Of (C566076) ..Temtamy preaxial brachydactyly syndrome (C536958) ..Tooth Agenesis, Selective, 2 (C566513) ..Tooth Agenesis, Selective, 3 (C567036) ..Tooth Agenesis, Selective, 4 (C563634) ..Tooth Agenesis, Selective, 5 (C565757) ..Tooth Agenesis, Selective, 6 (C567755) ..Tooth Agenesis, Selective, X-Linked, 1 (C567060) ..Tooth, Supernumerary (D014096) 3 ..Tricho-dento-osseous syndrome 1 (C536550) ..TRICHODENTOOSSEOUS SYNDROME (OMIM:190320) ..Weyers acrofacial dysostosis (C536695) ..Zazam Sheriff Phillips syndrome (C536723) Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD
Term ID: 3195
Name: Dentin Dysplasia
Definition: An apparently hereditary disorder of dentin formation, marked by a normal appearance of coronal dentin associated with pulpal obliteration, faulty root formation, and a tendency for peripheral lesions without obvious cause. (From Dorland, 27th ed)
Alternative IDs:
ParentIDs: MESH:D014071
TreeNumbers: C07.650.800.260 |C07.793.700.260 |C16.131.850.800.260
Synonyms: Dentin Dysplasias |Dysplasia, Dentin |Dysplasias, Dentin
Slim Mappings: Congenital abnormality|Mouth disease
Reference:
MedGen: D003805
MeSH: D003805
OMIM: Genes: Phenotypes Disease Causing ClinVar Variants