Congenital muscular torticollis

Symptom Information:

Symptom ID: HPO:0005988
Synonyms:
Torticollis, congenital [HPO:0005988]
Congenital torticollis [Orphanet:14900]
Congenital torticollis (disorder) [Orphanet:14900]
Congenital anomaly of sternocleidomastoid muscle (disorder) [Orphanet:14900]
Congenital anomaly of sternocleidomastoid muscle [Orphanet:14900]
Torticollis, congenital [OMIM:Torticollis, congenital]
Congenital torticolli [Orphanet:14900]
Congenital torticollis [MedDRA:10010650]
Quality:
Cross references:
Orphanet:14900 "Congenital torticolli" [Orphanet:14900]
OMIM: "Torticollis, congenital" [OMIM:Torticollis, congenital]
UMLS:C0345380 "Congenital anomaly of sternocleidomastoid muscle" [Orphanet:14900]
UMLS:C0079352 "Congenital torticollis" [Orphanet:14900]
Is a (Direct Parents):
HPO         Abnormality of the musculature of the neck
MedDRA Musculoskeletal and connective tissue disorders of spine congenital
Orphanet Abnormality of the neck
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)
Database Frequency: 11 / 7739
Resource:

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)