Disease Browser
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Parent Node: Stomatognathic System Abnormalities (D018640) |
Parent Node: Tooth Diseases (D014076) |
..Starting node ..Tooth Abnormalities (D014071)
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Child Nodes:
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........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) |
Sister Nodes: |
..Bork Stender Schmidt syndrome (C536576)
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..Bruxism (D002012) 2
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..Dental Deposits (D003741) 3
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..Dental Leakage (D003763)
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..Dental Pulp Diseases (D003788) 8
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..Dentin Sensitivity (D003807)
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..Failure of Tooth Eruption, Primary (C565114)
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..Fluorosis, Dental (D009050)
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..Focal Infection, Dental (D005491)
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..Hypercementosis (D006936)
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..Hypoplasia of Teeth Roots (C564144)
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..Malocclusion (D008310) 9
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..Mouth, Edentulous (D009066) 2
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..Tooth Abnormalities (D014071) 130
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..Tooth Ankylosis (D020254) 1
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..Tooth Demineralization (D017001) 6
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..Tooth Discoloration (D014075) 1
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..Tooth Eruption, Ectopic (D014079)
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..Tooth Injuries (D018677) 3
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..Tooth Loss (D016388)
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..Tooth Resorption (D014091) 1
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..Tooth Wear (D057085) 3
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..Tooth, Impacted (D014095)
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..Tooth, Unerupted (D014097)
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..Toothache (D014098)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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