You have selected the view in English
| Descriptor English: | Neuromuscular Diseases | ||||||
| Descriptor Spanish: |
Enfermedades Neuromusculares
| ||||||
| Descriptor Portuguese: | Doenças Neuromusculares | ||||||
| Descriptor French: | Maladies neuromusculaires | ||||||
| Entry term(s): |
Amyotonia Congenita Benign Fasciculation-Cramp Syndrome Benign Fasciculation-Cramp Syndromes Cramp Fasciculation Syndrome Cramp-Fasciculation Syndrome Cramp-Fasciculation Syndromes Fasciculation Cramp Syndrome, Benign Fasciculation-Cramp Syndrome, Benign Fasciculation-Cramp Syndromes, Benign Foley Denny Brown Syndrome Foley-Denny-Brown Syndrome Neuromuscular Disease Oppenheim Disease Oppenheim's Disease Oppenheims Disease Syndrome, Cramp-Fasciculation Syndrome, Foley-Denny-Brown Syndromes, Cramp-Fasciculation |
||||||
| Tree number(s): |
C10.668 |
||||||
| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D009468 | ||||||
| Scope note: | 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. |
||||||
| Annotation: | general or unspecified; prefer specifics; do not confuse entry term AMYOTONIA CONGENITA with MYOTONIA CONGENITA |
||||||
| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
||||||
| Previous Indexing: |
Muscular Diseases (1966-1970) Nervous System Diseases (1966-1970) |
||||||
| Public MeSH Note: | 1971; AMYOTONIA CONGENITA was heading 1963-96; for MYATONIA CONGENITA & OPPENHEIM'S DISEASE see AMYOTONIA CONGENITA 1963-1996 |
||||||
| History Note: | 1971; AMYOTONIA CONGENITA was heading 1963-96 |
||||||
| Entry Version: | NEUROMUSCULAR DIS |
||||||
| DeCS ID: | 9660 | ||||||
| Unique ID: | D009468 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1971/01/01 | ||||||
| Date of Entry: | 1999/01/01 | ||||||
| Revision Date: | 2012/07/03 |
|
|
Neuromuscular Diseases
- Preferred
Foley-Denny-Brown Syndrome
- Narrower
Oppenheim Disease
- Related but not broader or narrower
| Concept UI |
M0014726 |
| Scope note | 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. |
| Preferred term | Neuromuscular Diseases |
| Entry term(s) |
Neuromuscular Disease |
| Concept UI |
M0337845 |
| Preferred term | Foley-Denny-Brown Syndrome |
| Entry term(s) |
Benign Fasciculation-Cramp Syndrome Benign Fasciculation-Cramp Syndromes Cramp Fasciculation Syndrome Cramp-Fasciculation Syndrome Cramp-Fasciculation Syndromes Fasciculation Cramp Syndrome, Benign Fasciculation-Cramp Syndrome, Benign Fasciculation-Cramp Syndromes, Benign Foley Denny Brown Syndrome Syndrome, Cramp-Fasciculation Syndrome, Foley-Denny-Brown Syndromes, Cramp-Fasciculation |
| Concept UI |
M0014725 |
| Preferred term | Oppenheim Disease |
| Entry term(s) |
Amyotonia Congenita Oppenheim's Disease Oppenheims Disease |
We want your feedback on the new DeCS / MeSH website
We invite you to complete a survey that will take no more than 3 minutes.
Go to survey
