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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
chondrodysplasia Blomstrand type  
Dermochondrocorneal Dystrophy of François 
Dysplasia Epiphysealis Hemimelica with Chondromas and Osteochondromas 
Exostoses of Heel 
Intestinal Polyposis with Multiple Exostoses 
Kniest Like Dysplasia Lethal  
metachondromatosis  
Metaphyseal Acroscyphodysplasia 
Multiple Exostoses Type I  
Multiple Exostoses Type II  
Hereditary multiple exostoses is an autosomal dominant disorder characterized by multiple exostoses most commonly arising from the juxtaepiphyseal region of the long bones. Multiple hereditary exostoses type II (EXT2) is caused by heterozygous mutation in the gene encoding exostosin-2 (EXT2) on chromosome 11p11. (OMIM)
Multiple Exostoses Type III 
Multiple Exostoses with Spastic Tetraparesis 
Potocki-Shaffer syndrome  
Stuve-Wiedemann Syndrome +   

Synonyms
Exact Synonyms: EXT2 ;   hereditary multiple exostoses 2 ;   multiple exostoses type 2
Primary IDs: MIM:133701

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