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Ontology Browser
Term:
Oculodentodigital Dysplasia, Autosomal Recessive (DOID:9004641)
Annotations: Rat: (2) Mouse: (2) Human: (2) Chinchilla: (2) Bonobo: (2) Dog: (2) Squirrel: (2) Pig: (2) Naked Mole-rat: (2) Green Monkey: (2)
Parent Terms Term With Siblings Child Terms
Adams Nance Syndrome 
Alaninuria with Microcephaly, Dwarfism, Enamel Hypoplasia, and Diabetes Mellitus 
amelogenesis imperfecta +   
Ameloonychohypohidrotic Syndrome 
Arhinia, Choanal Atresia, and Microphthalmia  
Aughton Syndrome 
Behrens Baumann Dust Syndrome 
cataract 40  
chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia  
COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS  
Duker Weiss Siber syndrome 
Enamel Hypoplasia, Cataracts, and Aqueductal Stenosis 
Facial Hemihypertrophy +   
Fronto-Facio-Nasal Dysplasia 
frontonasal dysplasia 3  
GARG-MISHRA PROGEROID SYNDROME  
Ghose Sachdev Kumar Syndrome 
GOMBO Syndrome 
HEART AND BRAIN MALFORMATION SYNDROME  
Hemifacial Hyperplasia with Strabismus 
Hemifacial Myohyperplasia  
Hereditary Congenital Facial Paresis +   
Hittner Hirsch Kreh Syndrome  
Holoprosencephaly 10  
isolated microphthalmia +   
Kaplowitz Bodurtha syndrome 
Macrosomia with Lethal Microphthalmia 
Mehes Syndrome 
Microcephaly Microphthalmos Blindness 
Microcornea Corectopia Macular Hypoplasia 
Microcornea, Myopic Chorioretinal Atrophy, and Telecanthus  
Microgastria Limb Reduction Defect 
Microphthalmia and Mental Deficiency 
Microphthalmia Associated with Colobomatous Cyst 
Microphthalmia with Cyst, Bilateral Facial Clefts, and Limb Anomalies 
Microphthalmia with Hyperopia, Retinal Degeneration, Macrophakia, and Dental Anomalies 
Microphthalmia, Cataracts, and Iris Abnormalities  
nanophthalmos +   
Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia 
Oculodentodigital Dysplasia, Autosomal Recessive  
Opitz Reynolds Fitzgerald syndrome 
optic disc anomalies with retinal and/or macular dystrophy  
Pfeiffer Palm Teller Syndrome 
Seow Najjar Syndrome 
Singleton Merten Syndrome +   
syndromic microphthalmia +   
Tachycardia, Hypertension, Microphthalmia, And Hyperglycinuria 
Thomas Jewett Raines Syndrome 
trichodontoosseous syndrome  
Trichoodontoonychial Dysplasia 

Synonyms
Exact Synonyms: ODDD, autosomal recessive ;   ODOD, autosomal recessive ;   oculodentodigital dysplasia, autosomal recessive ;   oculodentoosseous dysplasia, autosomal recessive ;   oculodentoosseous dysplasia, recessive
Primary IDs: MESH:C567605
Alternate IDs: MESH:C537733 ;   OMIM:257850

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