Neck flexor weakness
Symptom Information:
Symptom ID: | HPO:0003722 | |||||
Synonyms: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the musculature(HPO:0003011) Abnormality of the musculature of the neck(HPO:0011006) Neck muscle weakness(HPO:0000467) Neck flexor weakness(HPO:0003722) Abnormality of muscle physiology(HPO:0011804) Muscle weakness(HPO:0001324) Neck muscle weakness(HPO:0000467) Neck flexor weakness(HPO:0003722) Abnormality of head or neck(HPO:0000152) Abnormality of the neck(HPO:0000464) Abnormality of the musculature of the neck(HPO:0011006) Neck muscle weakness(HPO:0000467) Neck flexor weakness(HPO:0003722) MedDRA: |
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Database Frequency: | 13 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
Autosomal recessive limb-girdle muscular dystrophy type 2C | (Orphanet:353) |
Autosomal recessive limb-girdle muscular dystrophy type 2H | (Orphanet:1878) |
Autosomal recessive limb-girdle muscular dystrophy type 2M | (Orphanet:206554) |
Congenital myopathy with excess of thin filaments | (Orphanet:98904) |
Distal myopathy with early respiratory muscle involvement | (Orphanet:34521) |
Hereditary proximal myopathy with early respiratory failure | (Orphanet:178464) |
MYOPATHY, ISOLATED MITOCHONDRIAL, AUTOSOMAL DOMINANT | (OMIM:616209) |
NEMALINE MYOPATHY 2 | (OMIM:256030) |
NEMALINE MYOPATHY 6 | (OMIM:609273) |
Nemaline myopathy | (Orphanet:607) |
Proximal myotonic myopathy | (Orphanet:606) |
Spheroid body myopathy | (Orphanet:268129) |
VACUOLAR NEUROMYOPATHY | (OMIM:601846) |