Tendon rupture
Symptom Information:
Symptom ID: | HPO:0100550 | |||||||||||||||||||||||||||||||||||||||
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 tendon morphology(HPO:0100261) Tendon rupture(HPO:0100550) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Tendon, ligament and cartilage disorders(MedDRA:10043237) Tendon disorders(MedDRA:10043234) Tendon rupture(HPO:0100550) |
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Database Frequency: | 17 / 7739 | |||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Alkaptonuria | (Orphanet:56) |
Costello syndrome | (Orphanet:3071) |
Diffuse cutaneous systemic sclerosis | (Orphanet:220393) |
Ehlers-Danlos syndrome, hypermobility type | (Orphanet:285) |
Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
Enthesitis-related arthritis | (Orphanet:85438) |
Familial articular chondrocalcinosis | (Orphanet:1416) |
Immunoglobulin A vasculitis | (Orphanet:761) |
Juvenile idiopathic arthritis | (Orphanet:92) |
Limited cutaneous systemic sclerosis | (Orphanet:220402) |
Limited systemic sclerosis | (Orphanet:220407) |
Mixed connective tissue disease | (Orphanet:809) |
Mucopolysaccharidosis type 1 | (Orphanet:579) |
Oculocerebrorenal syndrome | (Orphanet:534) |
Reactive arthritis | (Orphanet:29207) |
Scleroderma | (Orphanet:801) |
Singleton-Merten dysplasia | (Orphanet:85191) |