Neck muscle weakness
Symptom Information:
Symptom ID: | HPO:0000467 | ||||
Synonyms: |
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Cross references: |
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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 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) Abnormality of the musculature(HPO:0003011) Abnormality of the musculature of the neck(HPO:0011006) Neck muscle weakness(HPO:0000467) Abnormality of muscle physiology(HPO:0011804) Muscle weakness(HPO:0001324) Neck muscle weakness(HPO:0000467) MedDRA: |
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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) |