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Ontology Browser

Term:
Microtia, Hearing Impairment, and Cleft Palate (DOID:9003920)
Annotations: Rat: (2) Mouse: (2) Human: (2) Chinchilla: (2) Bonobo: (2) Dog: (2) Squirrel: (2) Pig: (2)
Parent Terms Term With Siblings Child Terms
cleft palate +     
Hearing Loss +     
Aase Smith Syndrome 
Acromegaloid Features, Overgrowth, Cleft Palate, and Hernia 
Ankyloblepharon Filiforme Adnatum 
ankyloblepharon-ectodermal defects-cleft lip/palate syndrome  
Arthrogryposis, Cleft Palate, Craniosynostosis, and Impaired Intellectual Development  
Aughton Syndrome 
Baetz-Greenwalt syndrome 
Bamforth-Lazarus syndrome  
Baraitser Rodeck Garner syndrome 
Basel-Vanagaite-Smirin-Yosef syndrome  
Behr Syndrome  
blepharocheilodontic syndrome +   
Branchial Arch Syndrome X-Linked 
camptodactyly-tall stature-scoliosis-hearing loss syndrome  
Cardiac Malformation, Cleft Lip-Palate, Microcephaly and Digital Anomalies  
chromosome 6pter-p24 deletion syndrome 
Cleft Lip with or without Cleft Palate, Nonsyndromic, 7 
Cleft Palate with Ankyloglossia  
Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly 
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  
Coloboma of Macula and Skeletal Anomalies 
Combined Cerebellar and Peripheral Ataxia with Hearing Loss and Diabetes Mellitus  
Conductive Hearing Loss +   
Cone-Rod Dystrophy and Hearing Loss +   
Congenital Cataracts, Hearing Loss, and Neurodegeneration  
Congenital Deafness with Inner Ear Agenesis, Microtia, and Microdontia  
Congenital Hydronephrosis, with Cleft Palate, Characteristic Facies, Hypotonia, and Mental Retardation 
Congenital Symmetric Circumferential Skin Creases +   
Craniosynostosis Mental Retardation Clefting Syndrome 
Crumpled Helices and Small Mouth 
Deafness +   
Deafness, Autosomal Dominant, due to Mutation In Myo1a 
Deafness, Congenital Heart Defects, and Posterior Embryotoxon  
Deafness, Unilateral, with Delayed Endolymphatic Hydrops  
Deafness-Craniofacial Syndrome 
Diamond-Blackfan Anemia with Microtia and Cleft Palate  
Dyssegmental Dysplasia, Rolland-Desbuquois Type 
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1 
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3  
Ectrodactyly-Cleft Palate Syndrome 
EEC syndrome +   
EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2  
Emanuel Syndrome 
Epilepsy, Hearing Loss, and Mental Retardation Syndrome  
EVEN-PLUS SYNDROME  
Facial Dysmorphism, Cleft Palate, Hearing Loss, and Camptodactyly 
Faciocardiorenal Syndrome 
Familial Lissencephaly with Cleft Palate and Cerebellar Hypoplasia 
Familial Popliteal Pterygium Syndrome 
Feingold Trainer Syndrome 
Frontonasal Dysplasia 3  
Functional Hearing Loss 
Genito Palato Cardiac Syndrome 
Gordon Syndrome  
Halal Syndrome 
Hardikar Syndrome 
Hay Wells Syndrome Recessive Type 
Hearing Loss, Bilateral +   
Hearing Loss, Mixed Conductive-Sensorineural +  
Hearing Loss, Unilateral +   
High-Frequency Hearing Loss  
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 
Hypotrichosis, Progressive Patterned Scalp, with Wiry Hair, Onycholysis, and Cleft Lip/Palate 
Iida Kannari Syndrome 
Iris Dysplasia Hypertelorism Deafness 
isolated cleft palate  
Isotretinoin Embryopathy Like Syndrome 
Kallmann Syndrome 2 with Cleft Lip or Palate 
Kapur Toriello Syndrome 
Kniest dysplasia  
Kuster Syndrome 
LADD syndrome  
Ladda Zonana Ramer syndrome 
Larsen syndrome  
Lowry Maclean syndrome 
Macrosomia with Lethal Microphthalmia 
Martinez Monasterio Pinheiro Syndrome 
Mastocytosis, Cutaneous, with Short Stature, Conductive Hearing Loss and Microtia 
McPherson Clemens Syndrome 
Meier-Gorlin syndrome +   
Microcephaly, Corpus Callosum Dysgenesis and Cleft Lip-Palate 
Microcephaly, Growth Retardation, Cataract, Hearing Loss, and Unusual Appearance 
Microtia with Nasolacrimal Duct Imperforation and Eye Coloboma 
Microtia, Hearing Impairment, and Cleft Palate  
Microtia, Meatal Atresia and Conductive Deafness 
Microtia-Anotia  
MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS  
Mitochondrial Progressive Myopathy with Congenital Cataract, Hearing Loss, and Developmental Delay  
Multiple Epiphyseal Dysplasia with Robin Phenotype 
Native American myopathy  
Oculomaxillofacial Dysostosis  
Oculopalatocerebral Syndrome 
Omphalocele, Cleft Palate Syndrome Lethal 
Opitz GBBB Syndrome, Type I  
Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant 
Palant Cleft Palate Syndrome 
PARC Syndrome 
Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss  
Periventricular Nodular Heterotopia with Syndactyly, Cleft Palate and Developmental Delay  
Piepkorn Karp Hickok syndrome 
Pilotto Syndrome 
popliteal pterygium syndrome +   
Raine Syndrome  
Rapp-Hodgkin syndrome  
Reardon Hall Slaney syndrome 
Reardon Wilson Cavanagh Syndrome 
Rosselli-Gulienetti Syndrome 
Sakoda Complex 
Samson Viljoen Syndrome 
Say Syndrome 
Schilbach-Rott Syndrome Ocular Hypotelorism, Submucosal Cleft Palate, and Hypospadias 
Schrander-Stumpel Theunissen Hulsmans Syndrome 
Selective Tooth Agenesis with Orofacial Cleft 
sensorineural hearing loss +   
Seres-Santamaria Arimany Muniz Syndrome 
SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES  
Spondyloepiphyseal Dysplasia with Coronal Craniosynostosis, Cataracts, Cleft Palate, and Mental Retardation 
Spondylomegaepiphyseal Dysplasia with Upper Limb Mesomelia, Punctate Calcifications, and Deafness 
syndromic X-linked intellectual disability Abidi type 
uveal coloboma-cleft lip and palate-intellectual disability  
Van der Woude syndrome +   
Van der Woude Syndrome 2  
X-linked cleft palate with or without ankyloglossia  
Yim Ebbin Syndrome 
Zadik Barak Levin Syndrome 

Synonyms
Narrow Synonyms: MICROTIA WITH OR WITHOUT HEARING IMPAIRMENT
Primary IDs: MESH:C567359 ;   RDO:0015450
Alternate IDs: OMIM:612290

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