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Ontology Browser

Term:
Cleft Palate, Deafness, and Oligodontia (DOID:9007000)
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Parent Terms Term With Siblings Child Terms
anodontia +     
cleft palate +     
Aase Smith Syndrome 
Abruzzo-Erickson syndrome  
acheiropody  
Acromegaloid Features, Overgrowth, Cleft Palate, and Hernia 
Acrootoocular Syndrome 
ADULT syndrome  
Aloi Tomasini Isaia Syndrome 
Ankyloblepharon Filiforme Adnatum  
ankyloblepharon-ectodermal defects-cleft lip/palate syndrome  
Anodontia of Permanent Dentition  
Anonychia-Onychodystrophy with Hypoplasia or Absence of Distal Phalanges 
Arthrogryposis, Cleft Palate, Craniosynostosis, and Impaired Intellectual Development  
Aughton Syndrome 
Axenfeld-Rieger syndrome type 1  
Axenfeld-Rieger syndrome type 2 
Baetz-Greenwalt syndrome 
Bamforth-Lazarus syndrome  
Baraitser Rodeck Garner syndrome 
Basel-Vanagaite-Smirin-Yosef syndrome  
blepharocheilodontic syndrome +   
brachydactyly type E1  
brachydactyly type E2  
Brachymetapody-Anodontia-Hypotrichosis-Albinoidism 
Brachyphalangy, Polydactyly, and Tibial Aplasia/Hypoplasia 
Camptosynpolydactyly, Complex  
CAPOS Syndrome  
Cleft Lip with or without Cleft Palate, Nonsyndromic, 7 
Cleft Palate with Ankyloglossia  
Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly 
cleft palate, cardiac defects, and intellectual disabillity  
Cleft Palate, Deafness, and Oligodontia 
Cleft Palate, Midfacial Hypoplasia, Triangular Facies, and Sensorineural Hearing Loss 
Cleft Palate, Psychomotor Retardation, and Distinctive Facial Features  
cleft soft palate  
Cochlear Deafness with Myopia and Intellectual Impairment 
Coloboma of Macula and Skeletal Anomalies 
Conductive Stapedial Deafness with Ear Malformation and Facial Palsy 
Congenital Hydronephrosis, with Cleft Palate, Characteristic Facies, Hypotonia, and Mental Retardation 
Congenital Symmetric Circumferential Skin Creases +   
congenital vertical talus  
Craniosynostosis Mental Retardation Clefting Syndrome 
Craniosynostosis, Adelaide Type 
Crumpled Helices and Small Mouth 
Daneman Davy Mancer Syndrome 
Deafness Conductive Ptosis Skeletal Anomalies 
Deafness Oligodontia Syndrome 
Deafness, Conductive, with Malformed External Ear 
Deafness, Congenital Onychodystrophy, Recessive Form 
Dermatoosteolysis Kirghizian Type 
Diamond-Blackfan Anemia with Microtia and Cleft Palate 
Digitotalar Dysmorphism 
Dilated Cardiomyopathy with Woolly Hair, Keratoderma, and Tooth Agenesis  
distal arthrogryposis type 3  
Distal Symphalangism +   
Dysmyelinating Leukodystrophy with Oligodontia  
Dyssegmental Dysplasia, Rolland-Desbuquois Type 
Ectodermal Dysplasia, Trichoodontoonychial Type 
Ectrodactyly and Ectodermal Dysplasia without Cleft Lip/Palate 
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1 
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3  
Ectrodactyly-Cleft Palate Syndrome 
EEC syndrome +   
Eiken syndrome  
Emanuel Syndrome 
Facial Dysmorphism, Cleft Palate, Hearing Loss, and Camptodactyly 
Faciocardiorenal Syndrome 
Fairbank Disease 
Familial Lissencephaly with Cleft Palate and Cerebellar Hypoplasia 
Feingold Trainer Syndrome 
Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome 
Frias Syndrome 
Fried Goldberg Mundel Syndrome 
Frints De Smet Fabry Fryns Syndrome 
Frontonasal Dysplasia 3  
Fuhrmann syndrome  
Game Friedman Paradice Syndrome 
Genito Palato Cardiac Syndrome 
GOMBO Syndrome 
Growth Retardation, Alopecia, Pseudoanodontia and Optic Atrophy  
Growth Retardation, Small and Puffy Hands and Feet, and Eczema 
Hairy Palms and Soles 
Halal Syndrome 
hand-foot-genital syndrome  
Hardikar Syndrome 
Hay Wells Syndrome Recessive Type 
Ho Kaufman Mcalister Syndrome 
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate  
Holzgreve-Wagner-Rehder syndrome 
hypertelorism, microtia, facial clefting syndrome 
Hypodontia Oligodontia with Orofacial Cleft 
hypohidrotic ectodermal dysplasia +   
hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism  
Hypotrichosis, Progressive Patterned Scalp, with Wiry Hair, Onycholysis, and Cleft Lip/Palate 
Iida Kannari Syndrome 
isolated cleft palate  
Jackson-Weiss syndrome  
Johnson Munson Syndrome 
Kallmann Syndrome 2 with Cleft Lip or Palate 
Kapur Toriello Syndrome 
Kniest dysplasia  
Kuster Syndrome 
Ladda Zonana Ramer syndrome 
Larsen syndrome  
Late-Onset Localized Junctional Epidermolysis Bullosa with Mental Retardation 
Laurin-Sandrow syndrome  
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
Lowry Maclean syndrome 
Macrodactyly of the Foot 
Macrosomia with Lethal Microphthalmia 
Mammary-Digital-Nail Syndrome 
Martinez Monasterio Pinheiro Syndrome 
Mastocytosis, Cutaneous, with Short Stature, Conductive Hearing Loss and Microtia 
McPherson Clemens Syndrome 
Mehta Lewis Patton Syndrome 
Mengel Konigsmark Syndrome 
Metaphyseal Dysostosis, Mental Retardation, and Conductive Deafness 
Metatarsus Varus, Type I 
Microcephaly, Corpus Callosum Dysgenesis and Cleft Lip-Palate 
Microdontia Hypodontia Short Stature 
Microtia, Hearing Impairment, and Cleft Palate  
Microtia, Meatal Atresia and Conductive Deafness 
Mitral Regurgitation, Conductive Deafness, and Fusion of Cervical Vertebrae and of Carpal and Tarsal Bones  
Mononen-Karnes-Senac syndrome 
Monophalangy of Great Toe 
multiple epiphyseal dysplasia with myopia and deafness  
Multiple Epiphyseal Dysplasia with Robin Phenotype 
Native American myopathy  
Neural Deafness with Atypical Atopic Dermatitis 
Nicolaides Baraitser Syndrome  
oculodentodigital dysplasia +   
Oculopalatocerebral Syndrome 
Odontotrichoungual-Digital-Palmar Syndrome 
Oligodontia-Colorectal Cancer Syndrome  
Omphalocele, Cleft Palate Syndrome Lethal 
Opitz GBBB syndrome type I  
Oslam syndrome 
Palant Cleft Palate Syndrome 
PARC Syndrome 
Partial Aphalangia with Syndactyly and Duplication of Metatarsal IV 
Patterson Stevenson Syndrome  
Periventricular Nodular Heterotopia 7  
Pfeiffer Tietze Welte Syndrome 
Piepkorn Karp Hickok syndrome 
Pilotto Syndrome 
Pinheiro Freire-Maia Miranda Syndrome 
popliteal pterygium syndrome +   
Postaxial Polydactyly, with Dental and Vertebral Anomalies 
Preaxial Polydactyly II  
Progressive Deafness with Stapes Fixation 
Radial Defect Robin Sequence 
Radio-Ulnar Synostosis Type 1 
Radio-Ulnar Synostosis Type 2 
Raine Syndrome  
Rapp-Hodgkin syndrome  
Ray Peterson Scott Syndrome 
Reardon Hall Slaney syndrome 
Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism 
Richieri Costa Guion-Almeida Syndrome 
Rosselli-Gulienetti Syndrome 
Sakoda Complex 
Samson Viljoen Syndrome 
Sandhaus Ben-Ami Syndrome 
Say Syndrome 
Schilbach-Rott Syndrome 
Schopf-Schulz-Passarge syndrome  
Schrander-Stumpel Theunissen Hulsmans Syndrome 
Schweitzer Kemink Graham Syndrome 
Second Metatarsal-Metacarpal Syndrome 
Selective Tooth Agenesis with Orofacial Cleft 
Seres-Santamaria Arimany Muniz Syndrome 
Siegler Brewer Carey Syndrome 
solitary median maxillary central incisor  
Split Hand Split Foot Nystagmus 
split hand-foot malformation 1 with sensorineural hearing loss  
Split-Hand and Split-Foot With Hypodontia 
Spondyloepiphyseal Dysplasia with Coronal Craniosynostosis, Cataracts, Cleft Palate, and Mental Retardation 
Stoll Alembik Dott Syndrome 
Stoll Levy Francfort Syndrome 
Symphalangism with Multiple Anomalies of Hands and Feet 
syndromic microphthalmia 8  
Synpolydactyly 2  
Synpolydactyly with Foot Anomalies 
Talipes +   
Talonavicular Coalition 
Tarsal Coalition 
tarsal-carpal coalition syndrome  
Taurodontia, Absent Teeth, Sparse Hair 
Teebi Syndrome 
Terminal Osseous Dysplasia and Pigmentary Defects  
Thai Symphalangism Syndrome 
Thumb Deformity, Alopecia, Pigmentation Anomaly 
tooth and nail syndrome  
trichorhinophalangeal syndrome type III  
Trigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet 
Ulnar Hypoplasia Lobster Claw Deformity of Feet 
uveal coloboma-cleft lip and palate-intellectual disability  
Van der Woude syndrome +   
Van der Woude Syndrome 2  
Van Maldergem syndrome +   
X-linked cleft palate with or without ankyloglossia  
X-linked deafness 2  
X-Linked Hypodontia 
Yim Ebbin Syndrome 
Zadik Barak Levin Syndrome 
Zechi-Ceide Syndrome 
Zunich Neuroectodermal Syndrome  

Synonyms
Primary IDs: MESH:C565844
Alternate IDs: OMIM:216300

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