Torticollis
Symptom Information:
Symptom ID: | HPO:0000473 | ||||||||||||||||||||||||
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 the musculature(HPO:0003011) Abnormality of the musculature of the neck(HPO:0011006) Torticollis(HPO:0000473) 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 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) |
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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) |