Limited elbow movement
Symptom Information:
Symptom ID: | HPO:0002996 | |||||||
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) Limited elbow movement(HPO:0002996) Abnormal joint morphology(HPO:0001367) Abnormality of upper limb joint(HPO:0009810) Abnormality of the elbow(HPO:0009811) Limited elbow movement(HPO:0002996) Abnormality of joint mobility(HPO:0011729) Limitation of joint mobility(HPO:0001376) Limited elbow movement(HPO:0002996) MedDRA: |
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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) |