Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Ontology Browser

Term:
Multiple Exostoses Type II (DOID:9003693)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
chondrodysplasia Blomstrand type  
Dermochondrocorneal Dystrophy of Fran├žois 
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 ;   MULTIPLE EXOSTOSES TYPE 2 ;   hereditary multiple exostoses 2
Primary IDs: OMIM:133701
Alternate IDs: RDO:0007980

paths to the root

NHLBI Logo

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