A general term encompassing lower MOTOR NEURON DISEASE; PERIPHERAL NERVOUS SYSTEM
DISEASES; and certain MUSCULAR DISEASES. Manifestations include MUSCLE WEAKNESS; FASCICULATION;
muscle ATROPHY; SPASM; MYOKYMIA; MUSCLE HYPERTONIA, myalgias, and MUSCLE HYPOTONIA
Note générale sur le champ d'application :
GEN; do not confuse xref AMYOTONIA CONGENITA with MYOTONIA CONGENITA
Point d'accès autorisé parallèle
Neuromuscular Diseases
Autres identifiants
Identifiant MeSH : mesD009468
Utilisation dans FMeSH
Qualificatifs autorisés : DI / PS / IM / MI / DG / PP / RH / EN / ET / MO / EP / BL
/ CF / CI / CN / DH / DT / TH / PX / UR / VI / VE / HI / CL / CO / EC / EM / GE /
NU / RT / SU / EH / PC / PA / ME1971; AMYOTONIA CONGENITA was heading 1963-96