Humeroradial synostosis

Symptom Information:

Symptom ID: HPO:0003041
Synonyms:
Humeral radial synostosis [HPO:0003041]
Humeral-radial synostosis [HPO:0003041]
Radiohumeral synostosis of elbow [HPO:0003041]
Synostosis of radius and humerus [HPO:0003041]
Humeroradial joint synostosis [Orphanet:19540]
Humeroradial synostosis (disorder) [Orphanet:19540]
Humeroradial synostosis [Orphanet:19540]
Humeral-radial synostosis [OMIM:Humeral-radial synostosis]
Humeroradial synostosis [OMIM:Humeroradial synostosis]
Radiohumeral synostosis of elbow [OMIM:Radiohumeral synostosis of elbow]
Synostosis of radius and humerus [OMIM:Synostosis of radius and humerus]
Humeroradial fusion [Orphanet:19540]
Humeroradial fusion [OMIM:Humeroradial fusion]
Quality:
Cross references:
HPO:0003070 "Elbow ankylosis" [Orphanet:19540]
Orphanet:19540 "Humeroradial fusion" [Orphanet:19540]
OMIM: "Humeral-radial synostosis" [OMIM:Humeral-radial synostosis]
OMIM: "Humeroradial synostosis" [OMIM:Humeroradial synostosis]
OMIM: "Radiohumeral synostosis of elbow" [OMIM:Radiohumeral synostosis of elbow]
OMIM: "Synostosis of radius and humerus" [OMIM:Synostosis of radius and humerus]
OMIM: "Humeroradial fusion" [OMIM:Humeroradial fusion]
UMLS:C0431800 "Humeroradial synostosis" [Orphanet:19540]
Is a (Direct Parents):
HPO         Abnormality of the radius
HPO         Abnormality of the humerus
HPO         Abnormality of the humeroradial joint
HPO         Synostosis involving 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 the upper arm(HPO:0001454)
                         Abnormality of the humerus(HPO:0003063)
                            Humeroradial synostosis(HPO:0003041)
                      Abnormality of upper limb joint(HPO:0009810)
                         Synostosis involving bones of the upper limbs(HPO:0100238)
                            Synostosis involving the elbow(HPO:0003938)
                               Humeroradial synostosis(HPO:0003041)
                         Abnormality of the elbow(HPO:0009811)
                            Abnormality of the humeroradial joint(HPO:0100744)
                               Humeroradial synostosis(HPO:0003041)
                            Synostosis involving the elbow(HPO:0003938)
                               Humeroradial synostosis(HPO:0003041)
                      Abnormality of the forearm(HPO:0002973)
                         Abnormality of the radius(HPO:0002818)
                            Humeroradial synostosis(HPO:0003041)
             Abnormal joint morphology(HPO:0001367)
                Abnormality of joint mobility(HPO:0011729)
                   Synostosis of joints(HPO:0100240)
                      Synostosis involving bones of the upper limbs(HPO:0100238)
                         Synostosis involving the elbow(HPO:0003938)
                            Humeroradial synostosis(HPO:0003041)
                Abnormality of upper limb joint(HPO:0009810)
                   Synostosis involving bones of the upper limbs(HPO:0100238)
                      Synostosis involving the elbow(HPO:0003938)
                         Humeroradial synostosis(HPO:0003041)
                   Abnormality of the elbow(HPO:0009811)
                      Abnormality of the humeroradial joint(HPO:0100744)
                         Humeroradial synostosis(HPO:0003041)
                      Synostosis involving the elbow(HPO:0003938)
                         Humeroradial synostosis(HPO:0003041)
MedDRA:
Database Frequency: 19 / 7739
Resource:

All diseases associated with this symptom:

ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS (OMIM:201750)
Antley-Bixler syndrome (Orphanet:83)
Apert syndrome (Orphanet:87)
Femoral-facial syndrome (Orphanet:1988)
HUMERORADIAL SYNOSTOSIS (OMIM:143050)
HUMERORADIAL SYNOSTOSIS WITH CRANIOFACIAL ANOMALIES (OMIM:236410)
HUMERORADIAL SYNOSTOSISHUMERORADIAL/MULTIPLE SYNOSTOSIS SYNDROME, INCLUDED (OMIM:236400)
Humero-radial synostosis (Orphanet:3265)
Humero-radio-ulnar synostosis (Orphanet:3266)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
Lethal occipital encephalocele-skeletal dysplasia syndrome (Orphanet:293925)
MULTIPLE SYNOSTOSES SYNDROME 2 (OMIM:610017)
MULTIPLE SYNOSTOSES SYNDROME 3 (OMIM:612961)
Mietens syndrome (Orphanet:2557)
Pfeiffer syndrome (Orphanet:710)
Phocomelia, Schinzel type (Orphanet:2879)
Proximal symphalangism (Orphanet:3250)
TARSAL-CARPAL COALITION SYNDROME (OMIM:186570)
Ulbright-Hodes syndrome (Orphanet:3404)