Limited elbow flexion

Symptom Information:

Symptom ID: HPO:0006376
Synonyms:
Limited elbow flexion [OMIM:Limited elbow flexion]
Quality:
Cross references:
OMIM: "Limited elbow flexion" [OMIM:Limited elbow flexion]
Is a (Direct Parents):
HPO         Limited elbow flexion/extension
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 upper limb joint(HPO:0009810)
                   Abnormality of the elbow(HPO:0009811)
                      Limited elbow movement(HPO:0002996)
                         Limited elbow extension(HPO:0001377)
                            Limited elbow flexion/extension(HPO:0005060)
                               Limited elbow flexion(HPO:0006376)
                Abnormality of joint mobility(HPO:0011729)
                   Limitation of joint mobility(HPO:0001376)
                      Limited elbow movement(HPO:0002996)
                         Limited elbow extension(HPO:0001377)
                            Limited elbow flexion/extension(HPO:0005060)
                               Limited elbow flexion(HPO:0006376)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Abnormality of the upper limb(HPO:0002817)
                      Abnormality of upper limb joint(HPO:0009810)
                         Abnormality of the elbow(HPO:0009811)
                            Limited elbow movement(HPO:0002996)
                               Limited elbow extension(HPO:0001377)
                                  Limited elbow flexion/extension(HPO:0005060)
                                     Limited elbow flexion(HPO:0006376)
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive omodysplasia (Orphanet:93329)
Multiple epiphyseal dysplasia type 4 (Orphanet:93307)