Shoulder flexion contracture

Symptom Information:

Symptom ID: HPO:0003044
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
HPO         Abnormality of the shoulder
HPO         Contractures of the joints of the upper limbs
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       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)
                      Limb joint contracture(HPO:0003121)
                         Contractures of the joints of the upper limbs(HPO:0100360)
                            Shoulder flexion contracture(HPO:0003044)
             Abnormal axial skeleton morphology(HPO:0009121)
                Abnormality of the thorax(HPO:0000765)
                   Abnormality of the shoulder(HPO:0003043)
                      Shoulder flexion contracture(HPO:0003044)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of the shoulder(HPO:0003043)
                   Shoulder flexion contracture(HPO:0003044)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle morphology(HPO:0011805)
             Flexion contracture(HPO:0001371)
                Limb joint contracture(HPO:0003121)
                   Contractures of the joints of the upper limbs(HPO:0100360)
                      Shoulder flexion contracture(HPO:0003044)
       Abnormality of connective tissue(HPO:0003549)
          Flexion contracture(HPO:0001371)
             Limb joint contracture(HPO:0003121)
                Contractures of the joints of the upper limbs(HPO:0100360)
                   Shoulder flexion contracture(HPO:0003044)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Freeman-Sheldon syndrome (Orphanet:2053)
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 (Orphanet:2636)
NEMALINE MYOPATHY 5 (OMIM:605355)
Schwartz-Jampel syndrome (Orphanet:800)
WHISTLING FACE SYNDROME, RECESSIVE FORM (OMIM:277720)