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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Singleton-Merten Syndrome 1  
Any singleton-Merten dysplasia in which the cause of the disease is a mutation in the IFIH1 gene. (MONDO)
Singleton-Merten Syndrome 2  

Synonyms
Exact Synonyms: SGMRT1
Primary IDs: OMIM:182250
Xrefs: MONDO:0024535

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