Term info
database cross reference
- NCIT:C85027 (MONDO:equivalentTo)
- SCTID:88923002 (MONDO:equivalentTo)
- MESH:D009134 (MONDO:directSiblingOf)
- UMLS:C0917981 (Orphanet:454706)
- ICD9:335.21 (MONDO:i2s)
- EFO:0008864 (MONDO:equivalentTo)
- Orphanet:454706 (MONDO:equivalentTo)
- DOID:318 (MONDO:equivalentTo)
Subsets
ordo_disease
definition
A rare, milder form of amyotrophic lateral sclerosis. It is characterized by a slowly progressive clinical course. Signs and symptoms include muscle weakness, atrophy, and fasciculation.
exactMatch
http://purl.obolibrary.org/obo/DOID_318, http://purl.obolibrary.org/obo/Orphanet_454706, http://purl.obolibrary.org/obo/NCIT_C85027, http://identifiers.org/snomedct/88923002, http://linkedlifedata.com/resource/umls/id/C0917981
has exact synonym
progressive spinal muscular atrophy, PMA
has related synonym
pure progressive muscular atrophy
id
MONDO:0018687