Limited pronation/supination of forearm

Symptom Information:

Symptom ID: HPO:0006394
Synonyms:
Limited pronation/supination of forearm [OMIM:Limited pronation/supination of forearm]
Limited pronation and supination of forearms [OMIM:Limited pronation and supination of forearms]
Quality:
Cross references:
OMIM: "Limited pronation/supination of forearm" [OMIM:Limited pronation/supination of forearm]
OMIM: "Limited pronation and supination of forearms" [OMIM:Limited pronation and supination of forearms]
Is a (Direct Parents):
HPO         Limited elbow movement
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 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 pronation/supination of forearm(HPO:0006394)
             Abnormal joint morphology(HPO:0001367)
                Abnormality of upper limb joint(HPO:0009810)
                   Abnormality of the elbow(HPO:0009811)
                      Limited elbow movement(HPO:0002996)
                         Limited pronation/supination of forearm(HPO:0006394)
                Abnormality of joint mobility(HPO:0011729)
                   Limitation of joint mobility(HPO:0001376)
                      Limited elbow movement(HPO:0002996)
                         Limited pronation/supination of forearm(HPO:0006394)
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

OSTEOGENESIS IMPERFECTA, TYPE V (OMIM:610967)
Osteogenesis imperfecta type 5 (Orphanet:216828)
PRONATION-SUPINATION OF THE FOREARM, IMPAIRMENT OF (OMIM:176800)
Radio-ulnar synostosis - amegakaryocytic thrombocytopenia (Orphanet:71289)