Elbow ankylosis

Symptom Information:

Symptom ID: HPO:0003070
Synonyms:
Humeroradial joint synostosis [Orphanet:19540]
Humeroradial synostosis (disorder) [Orphanet:19540]
Humeroradial synostosis [Orphanet:19540]
Elbow ankylosis [OMIM:Elbow ankylosis]
Humeroradial fusion [Orphanet:19540]
Humeroradial fusion [OMIM:Humeroradial fusion]
Quality:
Cross references:
HPO:0003041 "Humeroradial synostosis" [Orphanet:19540]
Orphanet:19540 "Humeroradial fusion" [Orphanet:19540]
OMIM: "Elbow ankylosis" [OMIM:Elbow ankylosis]
OMIM: "Humeroradial fusion" [OMIM:Humeroradial fusion]
UMLS:C0431800 "Humeroradial synostosis" [Orphanet:19540]
Is a (Direct Parents):
HPO         Limitation of joint mobility
HPO         Abnormality of the elbow
Orphanet 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)
                            Elbow ankylosis(HPO:0003070)
             Abnormal joint morphology(HPO:0001367)
                Abnormality of joint mobility(HPO:0011729)
                   Limitation of joint mobility(HPO:0001376)
                      Elbow ankylosis(HPO:0003070)
                Abnormality of upper limb joint(HPO:0009810)
                   Abnormality of the elbow(HPO:0009811)
                      Elbow ankylosis(HPO:0003070)
MedDRA:
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

FETAL AKINESIA DEFORMATION SEQUENCE (OMIM:208150)
Fetal akinesia deformation sequence (Orphanet:994)
Isolated cloverleaf skull syndrome (Orphanet:2343)
KLEEBLATTSCHAEDEL (OMIM:148800)
Pfeiffer syndrome (Orphanet:710)
Phocomelia, Schinzel type (Orphanet:2879)
TARSAL-CARPAL COALITION SYNDROME (OMIM:186570)
Ulbright-Hodes syndrome (Orphanet:3404)