Degenerative joint disease
Symptom Information:
Symptom ID: | HPO:0001379 | ||||||
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 joint morphology(HPO:0001367) Degenerative joint disease(HPO:0001379) MedDRA: |
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Database Frequency: | 8 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Ehlers-Danlos syndrome, hypermobility type | (Orphanet:285) |
HEMOPHILIA A | (OMIM:306700) |
HEMOPHILIA A WITH VASCULAR ABNORMALITY | (OMIM:306800) |
Hemophilia B | (Orphanet:98879) |
Mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early-onset osteoarthritis | (Orphanet:93279) |
Pseudoachondroplasia | (Orphanet:750) |
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED | (OMIM:313400) |
TRICHORHINOPHALANGEAL SYNDROME, TYPE I | (OMIM:190350) |