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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
myopia +     
Aplasia Cutis Congenita, High Myopia, and Cone-Rod Dysfunction 
Blepharoptosis, Myopia, and Ectopia Lentis 
Bornholm Eye Disease 
Cochlear Deafness with Myopia and Intellectual Impairment 
Cohen syndrome  
congenital stationary night blindness +   
Dandy-Walker Malformation with Mental Retardation, Macrocephaly, Myopia, and Brachytelephalangy 
degenerative myopia  
Donnai-Barrow syndrome  
Epiphyseal Dysplasia of Femoral Head, Myopia, and Deafness 
External Ophthalmoplegia and Myopia 
Gastrocutaneous Syndrome 
Hamamy Syndrome  
High Myopia +   
Isolated Microphthalmia with Corectopia 
JOINT LAXITY, SHORT STATURE, AND MYOPIA  
MASS Syndrome  
Mousa Al din Al Nassar Syndrome 
multiple epiphyseal dysplasia with myopia and deafness  
Myopia 1 
Myopia 10 
Myopia 11 
Myopia 12 
Myopia 13 
Myopia 14 
Myopia 15 
Myopia 16 
Myopia 17, Autosomal Dominant 
Myopia 18, Autosomal Recessive 
Myopia 19, Autosomal Dominant 
Myopia 2  
Myopia 20, Autosomal Dominant 
Myopia, or nearsightedness, is a refractive error of the eye. Light rays from a distant object are focused in front of the retina and those from a near object are focused in the retina; therefore distant objects are blurry and near objects are clear. Myopia 20 maps to chromosome 13q12.12. (OMIM)
Myopia 21, Autosomal Dominant  
Myopia 22, Autosomal Dominant  
Myopia 23, Autosomal Recessive  
Myopia 24, Autosomal Dominant  
Myopia 25, Autosomal Dominant  
Myopia 26, X-Linked, Female-Limited  
Myopia 27  
Myopia 28  
Myopia 3 
Myopia 5 
Myopia 6  
Myopia 7 
Myopia 8 
Myopia 9 
Night Blindness Skeletal Anomalies Unusual Facies 
Noble Bass Sherman Syndrome 
Polydactyly Myopia Syndrome 
Sinus Node Disease and Myopia 
Spondyloepiphyseal Dysplasia, Myopia, and Sensorineural Deafness 

Synonyms
Exact Synonyms: MYP20
Primary IDs: MIM:614166

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