| Disease Browser
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Parent Node:
 Tooth Abnormalities (D014071) |
..Starting node
.. Carabelli Anomaly of Maxillary Molar Teeth (C566175)
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Child Nodes:
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Sister Nodes: |
..Ackerman syndrome (C538170)
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..Anodontia (D000848)  29
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..AREDYLD Syndrome (C537427)
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..Blepharo-cheilo-dontic syndrome (C536188)
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..Book Syndrome (C562993)
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..Carabelli Anomaly of Maxillary Molar Teeth (C566175)
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..Cleidocranial Dysplasia, Forme Fruste, Dental Anomalies Only (C563974)
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..CODAS syndrome (C536434)
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..Deafness with Labyrinthine Aplasia Microtia and Microdontia (LAMM) (C548011)
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..Deafness, Congenital, and Onychodystrophy, Autosomal Dominant (C567274)
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..Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia (C565195)
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..Dens in Dente (D003719) 1
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..Dental Enamel Hypoplasia (D003744) 29
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..Dentin Dysplasia (D003805) 3
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..Dentinogenesis Imperfecta (D003811) 7
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..Dermoodontodysplasia (C565103)
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..Diastema, Dental Medial (C565098)
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..Euhidrotic ectodermal dysplasia (C535763)
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..Facial Dysmorphism, Selective Tooth Agenesis, and Choroid Calcification (C567039)
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..Faciocardiomelic Dysplasia, Lethal (C565578)
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..Fused Teeth (D005671)
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..Grubben de Cock Borghgraef syndrome (C537621)
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..Hypoglossia-Hypodactylia (C566308)
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..Iridogoniodysgenesis, dominant type (C535536)
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..Kallmann Syndrome 2 with Selective Tooth Agenesis (C566948)
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..KBG syndrome (C537015)
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..Lacrimoauriculodentodigital syndrome (C538132)
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..Larsen syndrome, dominant type (C537873)
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..Nance-Horan syndrome (C538336)
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..Oculodentodigital Dysplasia (C563160)
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..Oculodentodigital Dysplasia, Autosomal Recessive (C567605)
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..Oculotrichodysplasia (C564934)
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..Odontodysplasia (D018126) 3
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..Odontomicronychial dysplasia (C537741)
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..Odontotrichoungual-Digital-Palmar Syndrome (C566598)
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..Oroacral Syndrome, Verloes-Koulischer Type (C566374)
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..Otodental Dysplasia (C563482)
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..Polydactyly, Postaxial, with Dental and Vertebral Anomalies (C564880)
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..Rodrigues blindness (C535865)
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..Spondyloepimetaphyseal Dysplasia With Abnormal Dentition (C566644)
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..Taurodontism (C536946)
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..Taurodontism, microdontia, and dens invaginatus (C536947)
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..Teeth noneruption of with maxillary hypoplasia and genu valgum (C536952)
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..Teeth, Odd Shapes Of (C566076)
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..Temtamy preaxial brachydactyly syndrome (C536958)
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..Tooth Agenesis, Selective, 2 (C566513)
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..Tooth Agenesis, Selective, 3 (C567036)
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..Tooth Agenesis, Selective, 4 (C563634)
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..Tooth Agenesis, Selective, 5 (C565757)
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..Tooth Agenesis, Selective, 6 (C567755)
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..Tooth Agenesis, Selective, X-Linked, 1 (C567060)
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..Tooth, Supernumerary (D014096) 3
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..Tricho-dento-osseous syndrome 1 (C536550)
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..TRICHODENTOOSSEOUS SYNDROME (OMIM:190320)
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..Weyers acrofacial dysostosis (C536695)
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..Zazam Sheriff Phillips syndrome (C536723)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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