Torticollis

Symptom Information:

Symptom ID: HPO:0000473
Synonyms:
Cervical dystonia [HPO:0000473]
Spasmodic torticollis [HPO:0000473]
Spasmodic torticollis [Orphanet:43260]
Wry neck/torticollis (disorder) [Orphanet:43260]
Spasmodic torticollis (disorder) [Orphanet:43260]
Cervical Dystonia [Orphanet:43260]
Cervical dystonia [OMIM:Cervical dystonia]
Torticollis [OMIM:Torticollis]
Dystonia/torticollis/writer's cramp/blepharospasms [Orphanet:43260]
Cervical dystonia [Orphanet:43260]
Torticollis [Orphanet:43260]
Torticollis [MedDRA:10044074]
Spasmodic torticollis [MedDRA:10044074]
Torticollis (excl congenital, psychogenic and traumatic) [MedDRA:10044074]
Torticollis spastic [MedDRA:10044074]
Torticollis, unspecified [MedDRA:10044074]
Wry neck [MedDRA:10044074]
Wryneck [MedDRA:10044074]
Torticollis aggravated [MedDRA:10044074]
Retrocollis [MedDRA:10044074]
Cervical dystonia [MedDRA:10044074]
Antecollis [MedDRA:10044074]
Acute torticollis [MedDRA:10044074]
Torticollis (in some patients) [OMIM:Torticollis (in some patients)]
Quality:
Cross references:
Orphanet:43260 "Dystonia/torticollis/writer's cramp/blepharospasms" [Orphanet:43260]
OMIM: "Cervical dystonia" [OMIM:Cervical dystonia]
OMIM: "Torticollis" [OMIM:Torticollis]
OMIM: "Torticollis (in some patients)" [OMIM:Torticollis (in some patients)]
UMLS:C0040485 "Torticollis" [HPO:0000473]
UMLS:C0152116 "Spasmodic torticollis" [Orphanet:43260]
UMLS:C0949445 "Cervical Dystonia" [Orphanet:43260]
Is a (Direct Parents):
HPO         Abnormality of the musculature of the neck
HPO         Craniofacial dystonia
HPO         Abnormality of central motor function
Orphanet Abnormality of movement
MedDRA Muscle tone abnormalities
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system physiology(HPO:0012638)
             Abnormality of movement(HPO:0100022)
                Dystonia(HPO:0001332)
                   Focal dystonia(HPO:0004373)
                      Craniofacial dystonia(HPO:0012179)
                         Torticollis(HPO:0000473)
             Abnormality of central motor function(HPO:0011442)
                Torticollis(HPO:0000473)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of the musculature of the neck(HPO:0011006)
             Torticollis(HPO:0000473)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the neck(HPO:0000464)
             Abnormality of the musculature of the neck(HPO:0011006)
                Torticollis(HPO:0000473)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Muscle disorders(MedDRA:10028302)
       Muscle tone abnormalities(MedDRA:10028343)
          Torticollis(HPO:0000473)
Database Frequency: 42 / 7739
Resource:

All diseases associated with this symptom:

3MC SYNDROME 2 (OMIM:265050)
Aceruloplasminemia (Orphanet:48818)
Arthrogryposis multiplex congenita (Orphanet:1037)
Autosomal dominant cervical dystonia (Orphanet:93962)
Autosomal dominant dopa-responsive dystonia (Orphanet:98808)
Autosomal dominant focal dystonia, DYT25 (Orphanet:329466)
Autosomal dominant focal dystonia, DYT7 type (Orphanet:93963)
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA (OMIM:609945)
Bethlem myopathy (Orphanet:610)
CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III (OMIM:611929)
Congenital muscular dystrophy, Ullrich type (Orphanet:75840)
DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT (OMIM:128100)
DYSTONIA 17, TORSION, AUTOSOMAL RECESSIVE (OMIM:612406)
DYSTONIA 23 (OMIM:614860)
DYSTONIA 24 (OMIM:615034)
DYSTONIA WITH CEREBELLAR ATROPHY (OMIM:611694)
Dyschromatosis symmetrica hereditaria (Orphanet:41)
Dystonia 16 (Orphanet:210571)
Early-onset generalized limb-onset dystonia (Orphanet:256)
Kufor-Rakeb syndrome (Orphanet:306674)
Leber plus disease (Orphanet:99718)
Leukoencephalopathy - dystonia - motor neuropathy (Orphanet:163684)
MELAS (Orphanet:550)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 5 (OMIM:612621)
MESOAXIAL HEXADACTYLY AND CARDIAC MALFORMATION (OMIM:249670)
Mohr-Tranebjaerg syndrome (Orphanet:52368)
Myoclonus-dystonia syndrome (Orphanet:36899)
Niemann-Pick disease type C (Orphanet:646)
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (Orphanet:363972)
PAROXYSMAL NONKINESIGENIC DYSKINESIA 1 (OMIM:118800)
Parkinsonim due to ATP13A2 deficiency (Orphanet:314632)
Paroxysmal non-kinesigenic dyskinesia (Orphanet:98810)
Primary dystonia, DYT13 type (Orphanet:98807)
Primary dystonia, DYT2 type (Orphanet:99657)
Primary dystonia, DYT21 type (Orphanet:306734)
Primary dystonia, DYT4 type (Orphanet:98805)
Primary dystonia, DYT6 type (Orphanet:98806)
Rapid-onset dystonia-parkinsonism (Orphanet:71517)
SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY (OMIM:181405)
Spinocerebellar ataxia type 35 (Orphanet:276193)
TORTICOLLIS (OMIM:189600)
Torticollis - keloids - cryptorchidism - renal dysplasia (Orphanet:3341)