Arthralgia of the hip

Symptom Information:

Symptom ID: HPO:0003365
Synonyms:
Arthralgia (hip) [HPO:0003365]
Coxalgia [HPO:0003365]
Arthralgia (hip) [OMIM:Arthralgia (hip)]
Arthralgia (hands, feet, ankles, and knees) [OMIM:Arthralgia (hands, feet, ankles, and knees)]
Arthralgia (in some patients) [OMIM:Arthralgia (in some patients)]
Arthralgia (knee) [OMIM:Arthralgia (knee)]
Quality:
Cross references:
OMIM: "Arthralgia (hip)" [OMIM:Arthralgia (hip)]
OMIM: "Arthralgia (hands, feet, ankles, and knees)" [OMIM:Arthralgia (hands, feet, ankles, and knees)]
OMIM: "Arthralgia (in some patients)" [OMIM:Arthralgia (in some patients)]
OMIM: "Arthralgia (knee)" [OMIM:Arthralgia (knee)]
Is a (Direct Parents):
HPO         Abnormality of the hip bone
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 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)
                Abnormality of pelvic girdle bone morphology(HPO:0002644)
                   Abnormality of the hip bone(HPO:0003272)
                      Arthralgia of the hip(HPO:0003365)
MedDRA:
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)