Congenital muscular torticollis
Symptom Information:
Symptom ID: | HPO:0005988 | ||||||||
Synonyms: |
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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) Congenital muscular torticollis(HPO:0005988) Abnormality of head or neck(HPO:0000152) Abnormality of the neck(HPO:0000464) Abnormality of the musculature of the neck(HPO:0011006) Congenital muscular torticollis(HPO:0005988) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Musculoskeletal and connective tissue disorders congenital(MedDRA:10028396) Musculoskeletal and connective tissue disorders of spine congenital(MedDRA:10028383) Congenital muscular torticollis(HPO:0005988) |
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Database Frequency: | 11 / 7739 | ||||||||
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All diseases associated with this symptom:
Arthrogryposis due to muscular dystrophy | (Orphanet:1155) |
Bethlem myopathy | (Orphanet:610) |
Braddock syndrome | (Orphanet:52047) |
Distal trisomy 15q | (Orphanet:1707) |
Isolated Klippel-Feil syndrome | (Orphanet:2345) |
Malignant hyperthermia - arthrogryposis - torticollis | (Orphanet:2215) |
Microgastria - limb reduction defect | (Orphanet:2538) |
Neurogenic arthrogryposis multiplex congenita | (Orphanet:1143) |
Postaxial polydactyly - dental and vertebral anomalies | (Orphanet:2916) |
Torticollis - keloids - cryptorchidism - renal dysplasia | (Orphanet:3341) |
Trichodermal syndrome - intellectual deficit | (Orphanet:3360) |