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Ontology Browser

Term:
Spondyloepimetaphyseal Dysplasia with Abnormal Dentition (DOID:9001889)
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Parent Terms Term With Siblings Child Terms
Ackerman Syndrome 
Anauxetic Dysplasia +   
anodontia +   
anterior segment dysgenesis 4  
AREDYLD Syndrome 
autosomal dominant congenital deafness with onychodystrophy  
blepharocheilodontic syndrome +   
Book Syndrome 
Carabelli Anomaly of Maxillary Molar Teeth 
Cleidocranial Dysplasia, Forme Fruste, Dental Anomalies Only  
CODAS syndrome  
Congenital Deafness with Inner Ear Agenesis, Microtia, and Microdontia  
Craniosynostosis and Dental Anomalies  
Dens in Dente +  
dental enamel hypoplasia +   
dentin dysplasia +   
dentinogenesis imperfecta +   
Dermoodontodysplasia 
Diastema +  
Dilated Cardiomyopathy with Woolly Hair, Keratoderma, and Tooth Agenesis  
Dyggve-Melchior-Clausen disease +   
Euhidrotic Ectodermal Dysplasia 
Fused Teeth 
Grubben de Cock Borghgraef Syndrome 
Hypoglossia-Hypodactylia 
HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME  
KBG syndrome  
LADD syndrome  
Larsen syndrome  
Lethal Faciocardiomelic Dysplasia 
Liberfarb Syndrome  
metatropic dysplasia  
Nance-Horan syndrome  
oculodentodigital dysplasia +   
Oculoskeletodental Syndrome  
Oculotrichodysplasia 
Odd Shapes of Teeth 
Odontodysplasia +   
Odontomicronychial Dysplasia 
Odontotrichoungual-Digital-Palmar Syndrome 
Oroacral Syndrome, Verloes-Koulischer Type 
Otodental Dysplasia 
Postaxial Polydactyly, with Dental and Vertebral Anomalies 
Rodrigues Blindness 
Schimke immuno-osseous dysplasia  
Spondyloepimetaphyseal Dysplasia with Abnormal Dentition 
Spondyloepimetaphyseal Dysplasia with Hypotrichosis 
Spondyloepimetaphyseal Dysplasia with Joint Laxity +   
SPONDYLOEPIMETAPHYSEAL DYSPLASIA, DI ROCCO TYPE  
Spondyloepimetaphyseal Dysplasia, Faden-Alkuraya Type  
spondyloepimetaphyseal dysplasia, Genevieve-type  
Spondyloepimetaphyseal Dysplasia, Irapa Type 
Spondyloepimetaphyseal Dysplasia, Isidor-Toutain Type  
Spondyloepimetaphyseal Dysplasia, Krakow Type  
Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related  
spondyloepimetaphyseal dysplasia, Missouri type  
spondyloepimetaphyseal dysplasia, Pakistani type  
Spondyloepimetaphyseal Dysplasia, Shohat Type  
spondyloepimetaphyseal dysplasia, Sponastrime type  
spondyloepimetaphyseal dysplasia, Strudwick type  
Spondyloepimetaphyseal Dysplasia, X-Linked  
spondyloepiphyseal dysplasia congenita  
spondyloepiphyseal dysplasia tarda +   
spondyloepiphyseal dysplasia with congenital joint dislocations  
Supernumerary Tooth +   
Taurodontism +  
Taurodontism, Microdontia, and Dens Invaginatus 
Teeth Noneruption of with Maxillary Hypoplasia and Genu Valgum 
temtamy preaxial brachydactyly syndrome  
tooth agenesis +   
Tricho-Dento-Osseous Syndrome 1 
Weyers acrofacial dysostosis  
X-linked Spondyloepimetaphyseal Dysplasia with Hypomyelinating Leukodystrophy   
Zazam Sheriff Phillips Syndrome 

Synonyms
Exact Synonyms: SEMDAD
Primary IDs: MESH:C566644
Alternate IDs: OMIM:601668 ;   RDO:0014949

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.