Arthralgia of the hip
Symptom Information:
Symptom ID: | HPO:0003365 | ||||||
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) Abnormality of lower limb joint(HPO:0100491) Abnormality of the hip bone(HPO:0003272) Arthralgia of the hip(HPO:0003365) Abnormal appendicular skeleton morphology(HPO:0011844) Abnormality of pelvic girdle bone morphology(HPO:0002644) Abnormality of the hip bone(HPO:0003272) Arthralgia of the hip(HPO:0003365) Abnormality of limb bone morphology(HPO:0002813) Abnormality of the lower limb(HPO:0002814) Abnormality of lower limb joint(HPO:0100491) Abnormality of the hip bone(HPO:0003272) Arthralgia of the hip(HPO:0003365) MedDRA: |
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Database Frequency: | 10 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Dermatoosteolysis, Kirghizian type | (Orphanet:1657) |
EPIPHYSEAL DYSPLASIA, MULTIPLE, 6 | (OMIM:614135) |
Gaucher disease type 1 | (Orphanet:77259) |
IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1 | (OMIM:161950) |
IgA NEPHROPATHY, SUSCEPTIBILITY TO, 2 | (OMIM:613944) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Multiple epiphyseal dysplasia type 5 | (Orphanet:93311) |
Multiple epiphyseal dysplasia, with severe proximal femoral dysplasia | (Orphanet:166029) |
Upington disease | (Orphanet:3408) |
WIDOW'S PEAK SYNDROME | (OMIM:314570) |