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Ontology Browser

Term:
Congenital Deafness with Inner Ear Agenesis, Microtia, and Microdontia (DOID:9005439)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
Ackerman Syndrome 
Acrootoocular Syndrome 
anodontia +   
Anterior Segment Dysgenesis 4  
AREDYLD Syndrome 
Arthrogryposis-like Hand Anomaly and Sensorineural Deafness 
Ataxia, Deafness, and Cardiomyopathy 
Athabaskan brainstem dysgenesis syndrome  
Auditory Neuropathy, Nonsyndromic Recessive 
autosomal dominant cerebellar ataxia, deafness and narcolepsy  
autosomal dominant nonsyndromic deafness +   
autosomal recessive nonsyndromic deafness +   
autosomal recessive spinocerebellar ataxia 19  
Axenfeld-Rieger Anomaly with Cardiac Defects and Sensorineural Hearing Loss 
Ayme-Gripp Syndrome  
BADS syndrome 
Bart-Pumphrey syndrome  
Bartter disease type 4A  
Bartter disease type 4b  
Bjornstad syndrome  
blepharocheilodontic syndrome +   
Book Syndrome 
Boudhina Yedes Khiari syndrome 
Brachydactyly, Intraventricular Septal Defect, and Deafness 
Brown-Vialetto-Van Laere syndrome +   
CAPOS Syndrome  
Carabelli Anomaly of Maxillary Molar Teeth 
Cataract Ataxia Deafness 
CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA  
Cerebellar Ataxia and Hypergonadotropic Hypogonadism 
Cerebellar Ataxia and Neurosensory Deafness 
Charcot-Marie-Tooth disease type 1E  
Charcot-Marie-Tooth disease type 2J  
Charcot-Marie-Tooth disease X-linked recessive 4  
Chitty Hall Baraitser Syndrome 
Chudley-Mccullough syndrome  
Cleft Palate, Midfacial Hypoplasia, Triangular Facies, and Sensorineural Hearing Loss 
Cleidocranial Dysplasia, Forme Fruste, Dental Anomalies Only  
Cochleosaccular Degeneration of the Inner Ear and Progressive Cataracts 
CODAS syndrome  
Combined Pituitary Hormone Deficiency, 3  
Congenital Deafness with Inner Ear Agenesis, Microtia, and Microdontia  
Congenital Deafness, and Onychodystrophy, Autosomal Dominant  
Congenital Deafness, with Total Albinism 
Congenital Ectodermal Dysplasia with Hearing Loss 
Corneal Dystrophy and Perceptive Deafness  
cortical deafness +   
craniofacial-deafness-hand syndrome  
Craniosynostosis and Dental Anomalies  
Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness  
De Hauwere syndrome 
Deafness Enamel Hypoplasia Nail Defects  
Deafness Oligodontia Syndrome 
Deafness, Aminoglycoside-Induced  
Deafness, High-Frequency Sensorineural, X-Linked  
Deafness, Mid-Tone Neural 
Deafness, Progressive High-Tone Neural 
Deafness, X-Linked 1  
Deafness, X-Linked 3 
Deafness, X-Linked 4  
Deafness, X-Linked 5  
deafness-intellectual disability, Martin-Probst type syndrome  
Dens in Dente +  
dental enamel hypoplasia +   
dentin dysplasia +   
dentinogenesis imperfecta +   
Dermoodontodysplasia 
Diamond-Blackfan Anemia with Microtia and Cleft Palate  
Diastema +  
Digitorenocerebral Syndrome  
dilated cardiomyopathy 1J  
Dilated Cardiomyopathy with Woolly Hair, Keratoderma, and Tooth Agenesis  
Distal Renal Tubular Acidosis with Progressive Nerve Deafness  
Distal Renal Tubular Acidosis, Autosomal Recessive, with Late-Onset Sensorineural Hearing Loss  
dominant optic atrophy plus syndrome  
Donnai-Barrow syndrome  
EAST syndrome  
Ectodermal Dysplasia and Neurosensory Deafness 
Ectodermal Dysplasia, Sensorineural Hearing Loss, and Distinctive Facial Features 
Ermine Phenotype 
Euhidrotic Ectodermal Dysplasia 
EVEN-PLUS SYNDROME  
Faciocardiomelic Dysplasia, Lethal 
Fitzsimmons Walson Mellor Syndrome 
Flynn Aird Syndrome 
Friedreich Ataxia, So-Called, with Optic Atrophy and Sensorineural Deafness 
Fused Teeth 
Gemignani Syndrome 
Generalized Lipodystrophy, with Mental Retardation, Deafness, Short Stature, and Slender Bones 
Gonadal Dysgenesis, XX Type, with Deafness +   
Griscelli syndrome +   
Grubben de Cock Borghgraef Syndrome 
Hearing Loss, Cisplatin-Induced  
Hearing Loss, Noise-Induced  
Hearing Loss, Unilateral Sensorineural  
HID Syndrome  
High-Frequency Hearing Loss  
histiocytosis-lymphadenopathy plus syndrome  
Hittner Hirsch Kreh Syndrome 
Homozygous 11p15-p14 Deletion Syndrome 
hypertelorism, microtia, facial clefting syndrome 
Hypoglossia-Hypodactylia 
hypoparathyroidism-deafness-renal disease syndrome  
HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME  
Insulin-Like Growth Factor I Deficiency  
Isotretinoin Embryopathy Like Syndrome 
Johanson-Blizzard syndrome  
KBG syndrome  
LADD syndrome  
Larsen syndrome  
Marshall syndrome +   
Mastocytosis, Cutaneous, with Short Stature, Conductive Hearing Loss and Microtia 
Meier-Gorlin syndrome +   
Microtia with Nasolacrimal Duct Imperforation and Eye Coloboma 
Microtia, Hearing Impairment, and Cleft Palate  
Microtia, Meatal Atresia and Conductive Deafness 
Microtia-Anotia  
MYH-9 related disease +   
Nance-Horan syndrome  
Nephropathy Deafness Hyperparathyroidism 
Nephropathy with Pretibial Epidermolysis Bullosa and Deafness  
Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia 
Nonsyndromic Sensorineural Hearing Loss  
ocular albinism with sensorineural deafness  
oculodentodigital dysplasia +   
Oculoskeletodental Syndrome  
Oculotrichodysplasia 
Odontodysplasia +   
Odontomicronychial Dysplasia 
Odontotrichoungual-Digital-Palmar Syndrome 
Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy 
Oroacral Syndrome, Verloes-Koulischer Type 
Otodental Dysplasia 
Otofacioosseous-Gonadal Syndrome 
otospondylomegaepiphyseal dysplasia  
palmoplantar keratoderma-deafness syndrome  
Paragangliomas with Sensorineural Hearing Loss  
Pendred syndrome  
Pfeiffer Kapferer Syndrome 
Pigmentary Retinopathy and Sensorineural Deafness  
Postaxial Polydactyly, with Dental and Vertebral Anomalies 
Premature Atherosclerosis with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease 
Presbycusis +   
Progressive Hearing Loss Stapes Fixation  
Progressive Nephropathy with Deafness 
Prune Belly Syndrome with Pulmonic Stenosis, Mental Retardation, and Deafness 
Retinitis Pigmentosa Inversa with Deafness 
Robinson Miller Bensimon Syndrome 
Rod-Cone Dystrophy, Sensorineural Deafness, and Fanconi-Type Renal Dysfunction 
Rodrigues Blindness 
Schaap Taylor Baraitser Syndrome 
Sensorineural Deafness and Male Infertility  
Sensorineural Deafness and Migraine  
Sensorineural Deafness with Hypertrophic Cardiomyopathy  
Sensorineural Deafness with Mild Renal Dysfunction  
Sensorineural Deafness with Peripheral Neuropathy and Arterial Disease 
Sensorineural Deafness, Autosomal-Mitochondrial Type  
Sensorineural Hearing Loss, Retinal Pigment Epithelium Lesions, Discolored Teeth 
Spastic Paraplegia, Sensorineural Deafness, Mental Retardation, and Progressive Nephropathy 
split hand-foot malformation 1 with sensorineural hearing loss  
Spondyloepimetaphyseal Dysplasia with Abnormal Dentition 
Spondyloepiphyseal Dysplasia, Myopia, and Sensorineural Deafness 
Sudden Hearing Loss  
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  
thiamine-responsive megaloblastic anemia syndrome  
tooth agenesis +   
Townes-Brocks syndrome +   
Treft Sanborn Carey Syndrome 
Tricho-Dento-Osseous Syndrome 1 
Tunglang Savage Bellman Syndrome 
Usher syndrome +   
uveal coloboma-cleft lip and palate-intellectual disability  
Vohwinkel syndrome  
Weyers Acrofacial Dysostosis  
Wolfram syndrome 2  
Wolfram syndrome, mitochondrial form 
X-linked nonsyndromic deafness +   
Zazam Sheriff Phillips Syndrome 

Synonyms
Exact Synonyms: Congenital Deafness with Labyrinthine Aplasia, Microtia, and Microdontia ;   Deafness with Labyrinthine Aplasia Microtia and Microdontia (LAMM) ;   Deafness with Lamm ;   Lamm Syndrome
Primary IDs: MESH:C565195
Alternate IDs: OMIM:610706 ;   RDO:0013907

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