Typical nemaline myopathy is a moderate neonatal form of nemaline myopathy (NM) characterized by facial and skeletal muscle weakness and mild respiratory involvement. [ Orphanet:171436 ]

This is just here as a test because I lose it

Term information

database cross reference
  • GARD:12822 (Orphanet:171436)
  • Orphanet:171436 (MONDO:equivalentTo)
Subsets

gard_rare, ordo_disease, rare, nord_rare, orphanet_rare

exactMatch

http://www.orpha.net/ORDO/Orphanet_171436

has related synonym

typical congenital nemaline myopathy

id

MONDO:0015737