Limited elbow movement

Symptom Information:

Symptom ID: HPO:0002996
Synonyms:
Decreased elbow mobility [HPO:0002996]
Limited elbow mobility [HPO:0002996]
Restricted elbow motion [HPO:0002996]
Decreased elbow mobility [OMIM:Decreased elbow mobility]
Limited elbow mobility [OMIM:Limited elbow mobility]
Limited elbow movement [OMIM:Limited elbow movement]
Restricted elbow motion [OMIM:Restricted elbow motion]
Quality:
Cross references:
OMIM: "Decreased elbow mobility" [OMIM:Decreased elbow mobility]
OMIM: "Limited elbow mobility" [OMIM:Limited elbow mobility]
OMIM: "Limited elbow movement" [OMIM:Limited elbow movement]
OMIM: "Restricted elbow motion" [OMIM:Restricted elbow motion]
Is a (Direct Parents):
HPO         Limitation of joint mobility
HPO         Abnormality of the elbow
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)
             Abnormal joint morphology(HPO:0001367)
                Abnormality of joint mobility(HPO:0011729)
                   Limitation of joint mobility(HPO:0001376)
                      Limited elbow movement(HPO:0002996)
                Abnormality of upper limb joint(HPO:0009810)
                   Abnormality of the elbow(HPO:0009811)
                      Limited elbow movement(HPO:0002996)
MedDRA:
Database Frequency: 16 / 7739
Resource:

All diseases associated with this symptom:

3MC SYNDROME 2 (OMIM:265050)
Baller-Gerold syndrome (Orphanet:1225)
CORNELIA DE LANGE SYNDROME 2 (OMIM:300590)
CORNELIA DE LANGE SYNDROME 3 (OMIM:610759)
Costello syndrome (Orphanet:3071)
Femoral-facial syndrome (Orphanet:1988)
IVIC syndrome (Orphanet:2307)
LEOPARD SYNDROME 1 (OMIM:151100)
Léri-Weill dyschondrosteosis (Orphanet:240)
Madelung deformity (Orphanet:35688)
Noonan syndrome with multiple lentigines (Orphanet:500)
PSEUDOARTHROGRYPOSIS (OMIM:177300)
Peters-plus syndrome (Orphanet:709)
Spondyloepiphyseal dysplasia congenita (Orphanet:94068)
URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME (OMIM:300280)
Ulna hypoplasia - intellectual deficit (Orphanet:2249)