three M syndrome 2

Preferred Label : three M syndrome 2;

MeSH note : also known as 3M2; associated with mutation in OBSL1;

Origin ID

C567862;

UMLS CUI

C2752041;

Currated CISMeF NLP mapping
- Three M syndrome 2 [OMIM Phenotype]
MeSH term(s) associated for indexing
- dwarfism [MeSH Descriptor]
- muscle hypotonia [MeSH Descriptor]
Record concept(s)
- three M syndrome 2 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Three M syndrome 2 [OMIM Phenotype]