Preferred Name |
Neuromuscular Diseases |
Synonyms |
Fasciculation Cramp Syndrome, Benign |
Definitions |
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. |
ID |
http://purl.bioontology.org/ontology/MESH/D009468 |
altLabel |
Fasciculation Cramp Syndrome, Benign Amyotonia Congenita Syndrome, Foley-Denny-Brown Cramp-Fasciculation Syndromes Foley-Denny-Brown Syndrome Syndrome, Cramp-Fasciculation Benign Fasciculation-Cramp Syndromes Cramp-Fasciculation Syndrome Fasciculation-Cramp Syndromes, Benign Foley Denny Brown Syndrome Neuromuscular Disease Oppenheim's Disease Fasciculation-Cramp Syndrome, Benign Syndromes, Cramp-Fasciculation Cramp Fasciculation Syndrome Oppenheim Disease Oppenheims Disease Benign Fasciculation-Cramp Syndrome |
AN |
general or unspecified; prefer specifics; do not confuse entry term AMYOTONIA CONGENITA with MYOTONIA CONGENITA |
AQL |
BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI |
cui |
C0027868 C0002735 C0751381 |
DC |
1 |
definition |
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. |
DX |
19710101 |
HN |
1971; AMYOTONIA CONGENITA was heading 1963-96 |
Inverse of AQ |
http://purl.bioontology.org/ontology/MESH/Q000401 http://purl.bioontology.org/ontology/MESH/Q000150 http://purl.bioontology.org/ontology/MESH/Q000188 http://purl.bioontology.org/ontology/MESH/Q000517 http://purl.bioontology.org/ontology/MESH/Q000201 http://purl.bioontology.org/ontology/MESH/Q000145 http://purl.bioontology.org/ontology/MESH/Q000503 http://purl.bioontology.org/ontology/MESH/Q000453 http://purl.bioontology.org/ontology/MESH/Q000208 http://purl.bioontology.org/ontology/MESH/Q000134 http://purl.bioontology.org/ontology/MESH/Q000821 http://purl.bioontology.org/ontology/MESH/Q000382 http://purl.bioontology.org/ontology/MESH/Q000601 http://purl.bioontology.org/ontology/MESH/Q000235 http://purl.bioontology.org/ontology/MESH/Q000523 http://purl.bioontology.org/ontology/MESH/Q000276 http://purl.bioontology.org/ontology/MESH/Q000191 http://purl.bioontology.org/ontology/MESH/Q000652 http://purl.bioontology.org/ontology/MESH/Q000662 http://purl.bioontology.org/ontology/MESH/Q000151 http://purl.bioontology.org/ontology/MESH/Q000628 http://purl.bioontology.org/ontology/MESH/Q000196 http://purl.bioontology.org/ontology/MESH/Q000534 http://purl.bioontology.org/ontology/MESH/Q000266 http://purl.bioontology.org/ontology/MESH/Q000532 http://purl.bioontology.org/ontology/MESH/Q000139 http://purl.bioontology.org/ontology/MESH/Q000378 http://purl.bioontology.org/ontology/MESH/Q000175 http://purl.bioontology.org/ontology/MESH/Q000000981 http://purl.bioontology.org/ontology/MESH/Q000097 http://purl.bioontology.org/ontology/MESH/Q000473 http://purl.bioontology.org/ontology/MESH/Q000451 http://purl.bioontology.org/ontology/MESH/Q000209 |
Machine permutation |
1971; AMYOTONIA CONGENITA was heading 1963-96; for MYATONIA CONGENITA & OPPENHEIM'S DISEASE see AMYOTONIA CONGENITA 1963-1996 |
Mapped from |
http://purl.bioontology.org/ontology/MESH/C565542 http://purl.bioontology.org/ontology/MESH/C536229 http://purl.bioontology.org/ontology/MESH/C000629404 http://purl.bioontology.org/ontology/MESH/C565544 http://purl.bioontology.org/ontology/MESH/C565543 |
MDA |
19990101 |
MMR |
20120703 |
MN |
C10.668 |
notation |
D009468 |
prefLabel |
Neuromuscular Diseases |
TERMUI |
T373390 T028217 T028218 T373389 T028214 T373391 T028216 |
TH |
NLM (1971) NLM (2000) NLM (1997) OMIM (2013) |
tui |
T019 T047 |
subClassOf |