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Ontology Browser

Term:
Craniosynostosis and Dental Anomalies (DOID:9001911)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
craniosynostosis +     
3MC syndrome 1  
Ackerman Syndrome 
acrocephalosyndactylia +   
anodontia +   
Anterior Segment Dysgenesis 4  
AREDYLD Syndrome 
Arthrogryposis, Cleft Palate, Craniosynostosis, and Impaired Intellectual Development  
Aurocephalosyndactyly 
Baller-Gerold syndrome  
Baraitser Rodeck Garner syndrome 
Beare-Stevenson cutis gyrata syndrome  
blepharocheilodontic syndrome +   
Bohring Syndrome  
Book Syndrome 
Brachycephaly, Trichomegaly, and Developmental Delay  
Calabro Syndrome 
Carabelli Anomaly of Maxillary Molar Teeth 
Cleidocranial Dysplasia, Forme Fruste, Dental Anomalies Only  
CODAS syndrome  
Cole-Carpenter syndrome +   
Congenital Deafness with Inner Ear Agenesis, Microtia, and Microdontia  
Congenital Deafness, and Onychodystrophy, Autosomal Dominant  
Craniosynostosis 2  
Craniosynostosis 3  
Craniosynostosis 4  
Craniosynostosis 5  
Craniosynostosis 6  
Craniosynostosis 7  
Craniosynostosis and Dental Anomalies  
Craniosynostosis Mental Retardation Clefting Syndrome 
Craniosynostosis Microcephaly with Chromosomal Breakage and Other Abnormalities 
Craniosynostosis Syndrome, Autosomal Recessive  
Craniosynostosis with Anomalies of the Cranial Base and Digits 
Craniosynostosis with Ectopia Lentis 
Craniosynostosis with Fibular Aplasia 
Craniosynostosis with Ocular Abnormalities and Hallucal Defects 
Craniosynostosis, Adelaide Type 
Craniosynostosis, Anal Anomalies, and Porokeratosis 
Craniosynostosis, Calcification of Basal Ganglia, and Facial Dysmorphism 
Craniosynostosis, Philadelphia Type 
Craniosynostosis-Mental Retardation Syndrome of Lin and Gettig 
Craniotelencephalic Dysplasia 
Crouzon syndrome +   
Dens in Dente +  
dental enamel hypoplasia +   
dentin dysplasia +   
dentinogenesis imperfecta +   
Dermoodontodysplasia 
Diastema +  
Dilated Cardiomyopathy with Woolly Hair, Keratoderma, and Tooth Agenesis  
Euhidrotic Ectodermal Dysplasia 
Faciocardiomelic Dysplasia, Lethal 
Fine-Lubinsky Syndrome 
Frontonasal Dysplasia 2  
Fused Teeth 
Genoa Syndrome 
Gillessen-Kaesbach-Nishimura Dysplasia  
Grubben de Cock Borghgraef Syndrome 
Hordnes Engebretsen Knudtson syndrome 
Hunter-McAlpine Syndrome 
Hypoglossia-Hypodactylia 
HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME  
Iida Kannari Syndrome 
Jackson-Weiss syndrome  
KBG syndrome  
Kleeblattschaedel Syndrome 
LADD syndrome  
Larsen syndrome  
Loeys-Dietz syndrome +   
Lowry Maclean syndrome 
Mehta Lewis Patton Syndrome 
Muenke syndrome  
Nance-Horan syndrome  
Nonsyndromic Trigonocephaly +   
oculodentodigital dysplasia +   
Oculoskeletodental Syndrome  
Oculotrichodysplasia 
Odontodysplasia +   
Odontomicronychial Dysplasia 
Odontotrichoungual-Digital-Palmar Syndrome 
Opitz Trigonocephaly Syndrome  
Oroacral Syndrome, Verloes-Koulischer Type 
Otodental Dysplasia 
Pfeiffer Tietze Welte Syndrome 
Piepkorn Karp Hickok syndrome 
Plagiocephaly and X-Linked Mental Retardation 
Postaxial Polydactyly, with Dental and Vertebral Anomalies 
Rodrigues Blindness 
Sagittal Craniosynostosis with Dandy-Walker Malformation and Hydrocephalus 
Scaphocephaly, Maxillary Retrusion, and Mental Retardation  
Sensenbrenner syndrome +   
Shprintzen Golberg Craniosynostosis  
Skeletal Dysplasia, San Diego Type 
Spondyloepimetaphyseal Dysplasia with Abnormal Dentition 
Spondyloepiphyseal Dysplasia with Coronal Craniosynostosis, Cataracts, Cleft Palate, and Mental Retardation 
Supernumerary Tooth +  
Taurodontism +  
Taurodontism, Microdontia, and Dens Invaginatus 
Teeth Noneruption of with Maxillary Hypoplasia and Genu Valgum 
Teeth, Odd Shapes of 
temtamy preaxial brachydactyly syndrome  
tooth agenesis +   
Tricho-Dento-Osseous Syndrome 1 
Trigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet 
Weyers Acrofacial Dysostosis  
Zazam Sheriff Phillips Syndrome 

Synonyms
Exact Synonyms: CRSDA ;   Kreiborg-Pakistani Syndrome
Primary IDs: OMIM:614188 ;   RDO:9000257

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