Neck flexor weakness

Symptom Information:

Symptom ID: HPO:0003722
Synonyms:
Neck flexion weakness [HPO:0003722]
Neck flexor muscle weakness [HPO:0003722]
Neck flexion weakness [OMIM:Neck flexion weakness]
Neck flexor muscle weakness [OMIM:Neck flexor muscle weakness]
Neck flexor weakness [OMIM:Neck flexor weakness]
Quality:
Cross references:
OMIM: "Neck flexion weakness" [OMIM:Neck flexion weakness]
OMIM: "Neck flexor muscle weakness" [OMIM:Neck flexor muscle weakness]
OMIM: "Neck flexor weakness" [OMIM:Neck flexor weakness]
Is a (Direct Parents):
HPO         Neck muscle weakness
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       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)
       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)
MedDRA:
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)