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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Weill-Marchesani Syndrome 1  
This disease is a rare connective tissue disorder characterized by short stature, brachydactyly, joint stiffness, eye anomalies, including microspherophakia, ectopia of the lenses, severe myopia, and glaucoma,
Weill-Marchesani Syndrome 2  
Weill-Marchesani Syndrome 3  
Weill-Marchesani Syndrome 4  

Synonyms
Exact Synonyms: ADAMTS10-RELATED CONDITION ;   WMS1
Primary IDs: OMIM:277600
Definition Sources: OMIM:277600

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