A group of rare genetic muscle disorders characterized by hypotonia, muscle weakness, and delayed development of motor skills. [ NCIT:P378 ]
This is just here as a test because I lose it
Term information
database
cross reference
- DOID:422 (MONDO:equivalentTo)
- NCIT:C84648 (MONDO:equivalentTo)
- MESH:D020914 (MONDO:equivalentTo)
- UMLS:C0752282 (NCIT:C84648)
Subsets
rare, inferred_rare
exactMatch
http://identifiers.org/mesh/D020914
http://purl.obolibrary.org/obo/NCIT_C84648
http://purl.obolibrary.org/obo/DOID_422
http://linkedlifedata.com/resource/umls/id/C0752282