Decreased cervical spine flexion due to contractures of posterior cervical muscles

Symptom Information:

Symptom ID: HPO:0004631
Synonyms:
Contracture of post-cervical muscles [HPO:0004631]
Contracture of post-cervical muscles [OMIM:Contracture of post-cervical muscles]
Decreased cervical spine flexion due to contractures of posterior cervical muscles [OMIM:Decreased cervical spine flexion due to contractures of posterior cervical muscles]
Quality:
Cross references:
OMIM: "Contracture of post-cervical muscles" [OMIM:Contracture of post-cervical muscles]
OMIM: "Decreased cervical spine flexion due to contractures of posterior cervical muscles" [OMIM:Decreased cervical spine flexion due to contractures of posterior cervical muscles]
Is a (Direct Parents):
HPO         Flexion contracture
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle morphology(HPO:0011805)
             Flexion contracture(HPO:0001371)
                Decreased cervical spine flexion due to contractures of posterior cervical muscles(HPO:0004631)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal joint morphology(HPO:0001367)
                Abnormality of joint mobility(HPO:0011729)
                   Flexion contracture(HPO:0001371)
                      Decreased cervical spine flexion due to contractures of posterior cervical muscles(HPO:0004631)
       Abnormality of connective tissue(HPO:0003549)
          Flexion contracture(HPO:0001371)
             Decreased cervical spine flexion due to contractures of posterior cervical muscles(HPO:0004631)
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant Emery-Dreifuss muscular dystrophy (Orphanet:98853)
Autosomal recessive Emery-Dreifuss muscular dystrophy (Orphanet:98855)
Emery-Dreifuss muscular dystrophy (Orphanet:261)
[DEL]EMERY-DREIFUSS MUSCULAR DYSTROPHY 1, X-LINKED (OMIM:310300)