Acetabular spurs

Symptom Information:

Symptom ID: HPO:0010454
Synonyms:
Acetabular spurs [OMIM:Acetabular spurs]
Acetabular spurs (infancy) [OMIM:Acetabular spurs (infancy)]
Quality:
Cross references:
OMIM: "Acetabular spurs" [OMIM:Acetabular spurs]
OMIM: "Acetabular spurs (infancy)" [OMIM:Acetabular spurs (infancy)]
Is a (Direct Parents):
HPO         Abnormality of the acetabulum
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)
                      Abnormality of the hip joint(HPO:0001384)
                         Abnormality of the acetabulum(HPO:0003170)
                            Acetabular spurs(HPO:0010454)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of pelvic girdle bone morphology(HPO:0002644)
                   Abnormality of the hip bone(HPO:0003272)
                      Abnormality of the hip joint(HPO:0001384)
                         Abnormality of the acetabulum(HPO:0003170)
                            Acetabular spurs(HPO:0010454)
                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)
                            Abnormality of the hip joint(HPO:0001384)
                               Abnormality of the acetabulum(HPO:0003170)
                                  Acetabular spurs(HPO:0010454)
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Ellis Van Creveld syndrome (Orphanet:289)
Short-rib thoracic dysplasia 3 with or without polydactyly (OMIM:613091)
Short-rib thoracic dysplasia 8 with or without polydactyly (OMIM:615503)
Spondyloperipheral dysplasia - short ulna (Orphanet:1856)