Dislocated radial head
Symptom Information:
Symptom ID: | HPO:0003083 | |||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) Abnormality of the humeroradial joint(HPO:0100744) Dislocated radial head(HPO:0003083) Elbow dislocation(HPO:0003042) Dislocated radial head(HPO:0003083) Abnormality of the forearm(HPO:0002973) Abnormality of the radius(HPO:0002818) Abnormality of the radial head(HPO:0003995) Dislocated radial head(HPO:0003083) Abnormal joint morphology(HPO:0001367) Abnormality of upper limb joint(HPO:0009810) Abnormality of the elbow(HPO:0009811) Abnormality of the humeroradial joint(HPO:0100744) Dislocated radial head(HPO:0003083) Elbow dislocation(HPO:0003042) Dislocated radial head(HPO:0003083) MedDRA: Injury, poisoning and procedural complications(MedDRA:10022117) Bone and joint injuries(MedDRA:10005942) Fractures and dislocations NEC(MedDRA:10027677) Dislocated radial head(HPO:0003083) |
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Database Frequency: | 35 / 7739 | |||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE | (OMIM:101800) |
Acrodysostosis with multiple hormone resistance | (Orphanet:280651) |
Auriculoosteodysplasia | (Orphanet:114) |
Autosomal dominant omodysplasia | (Orphanet:93328) |
Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA | (OMIM:609945) |
Bohring-Opitz syndrome | (Orphanet:97297) |
C syndrome | (Orphanet:1308) |
CEREBROOCULOFACIOSKELETAL SYNDROME 4 | (OMIM:610758) |
COFFIN-SIRIS SYNDROME | (OMIM:135900) |
CORNELIA DE LANGE SYNDROME 1 | (OMIM:122470) |
Coffin-Siris syndrome | (Orphanet:1465) |
Conductive deafness - ptosis - skeletal anomalies | (Orphanet:3236) |
Cornelia de Lange syndrome | (Orphanet:199) |
HAJDU-CHENEY SYNDROME | (OMIM:102500) |
MULTIPLE SYNOSTOSES SYNDROME 1 | (OMIM:186500) |
Mesomelic dysplasia, Savarirayan type | (Orphanet:85170) |
Mietens syndrome | (Orphanet:2557) |
Multiple epiphyseal dysplasia, Lowry type | (Orphanet:166016) |
Multiple synostoses syndrome | (Orphanet:3237) |
OSTEOGENESIS IMPERFECTA, TYPE XIII | (OMIM:614856) |
Omodysplasia | (Orphanet:2733) |
Otopalatodigital syndrome type 1 | (Orphanet:90650) |
Pelviscapular dysplasia | (Orphanet:93333) |
Proximal radioulnar synostosis | (Orphanet:3269) |
Radio-ulnar synostosis - intellectual deficit - hypotonia | (Orphanet:3270) |
Rubinstein-Taybi syndrome due to CREBBP mutations | (Orphanet:353277) |
SECKEL SYNDROME 1 | (OMIM:210600) |
SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES | (OMIM:602471) |
STEEL SYNDROME | (OMIM:615155) |
Seckel syndrome | (Orphanet:808) |
Shprintzen-Goldberg syndrome | (Orphanet:2462) |
Spondyloepimetaphyseal dysplasia with joint laxity | (Orphanet:93359) |
Spondyloepimetaphyseal dysplasia with multiple dislocations | (Orphanet:93360) |
Van den Ende-Gupta syndrome | (Orphanet:2460) |