Neck muscle weakness

Symptom Information:

Symptom ID: HPO:0000467
Synonyms:
Neck muscle weakness [OMIM:Neck muscle weakness]
Neck muscle weakness (1 patient) [OMIM:Neck muscle weakness (1 patient)]
Neck muscle weakness (in some patients) [OMIM:Neck muscle weakness (in some patients)]
Quality:
Cross references:
OMIM: "Neck muscle weakness" [OMIM:Neck muscle weakness]
OMIM: "Neck muscle weakness (1 patient)" [OMIM:Neck muscle weakness (1 patient)]
OMIM: "Neck muscle weakness (in some patients)" [OMIM:Neck muscle weakness (in some patients)]
Is a (Direct Parents):
HPO         Abnormality of the musculature of the neck
HPO         Muscle weakness
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle physiology(HPO:0011804)
             Muscle weakness(HPO:0001324)
                Neck muscle weakness(HPO:0000467)
          Abnormality of the musculature of the neck(HPO:0011006)
             Neck muscle weakness(HPO:0000467)
       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)
MedDRA:
Database Frequency: 29 / 7739
Resource:

All diseases associated with this symptom:

Alpha-crystallinopathy (Orphanet:98910)
BROWN-VIALETTO-VAN LAERE SYNDROME 1 (OMIM:211530)
BROWN-VIALETTO-VAN LAERE SYNDROME 2 (OMIM:614707)
Cap myopathy (Orphanet:171881)
Congenital muscular dystrophy due to LMNA mutation (Orphanet:157973)
Congenital myasthenic syndromes with glycosylation defect (Orphanet:353327)
Congenital myopathy with excess of thin filaments (Orphanet:98904)
Desminopathy (Orphanet:98909)
EMERY-DREIFUSS MUSCULAR DYSTROPHY 4, AUTOSOMAL DOMINANT (OMIM:612998)
EMERY-DREIFUSS MUSCULAR DYSTROPHY 7, AUTOSOMAL DOMINANT (OMIM:614302)
Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia (Orphanet:79091)
Laing distal myopathy (Orphanet:59135)
MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE (OMIM:609456)
MYASTHENIC SYNDROME, CONGENITAL, 12 (OMIM:610542)
MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL (OMIM:608930)
MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL (OMIM:616322)
MYASTHENIC SYNDROME, CONGENITAL, 4B, FAST-CHANNEL (OMIM:616324)
MYASTHENIC SYNDROME, CONGENITAL, 9, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY (OMIM:616325)
MYOPATHY, DISTAL, TATEYAMA TYPE (OMIM:614321)
Mitochondrial myopathy with reversible cytochrome C oxidase deficiency (Orphanet:254864)
NEMALINE MYOPATHY 1 (OMIM:609284)
NEMALINE MYOPATHY 2 (OMIM:256030)
NEMALINE MYOPATHY 4 (OMIM:609285)
NEMALINE MYOPATHY 7 (OMIM:610687)
Neutral lipid storage myopathy (Orphanet:98908)
Oculopharyngeal muscular dystrophy (Orphanet:270)
Riboflavin transporter deficiency (Orphanet:97229)
Spinocerebellar ataxia type 35 (Orphanet:276193)
X-linked centronuclear myopathy (Orphanet:596)