Osteolysis involving tarsal bones

Symptom Information:

Symptom ID: HPO:0006234
Synonyms:
Tarsal bone osteolysis [HPO:0006234]
Tarsal osteolysis [HPO:0006234]
Tarsal bone osteolysis [OMIM:Tarsal bone osteolysis]
Tarsal osteolysis [OMIM:Tarsal osteolysis]
Quality:
Cross references:
OMIM: "Tarsal bone osteolysis" [OMIM:Tarsal bone osteolysis]
OMIM: "Tarsal osteolysis" [OMIM:Tarsal osteolysis]
Is a (Direct Parents):
HPO         Osteolysis involving bones of the feet
HPO         Abnormality of the tarsal bones
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 bone structure(HPO:0003330)
                Osteolysis(HPO:0002797)
                   Osteolysis involving bones of the lower limbs(HPO:0009139)
                      Osteolysis involving bones of the feet(HPO:0009134)
                         Osteolysis involving tarsal bones(HPO:0006234)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Abnormality of the lower limb(HPO:0002814)
                      Osteolysis involving bones of the lower limbs(HPO:0009139)
                         Osteolysis involving bones of the feet(HPO:0009134)
                            Osteolysis involving tarsal bones(HPO:0006234)
                      Abnormality of the foot(HPO:0001760)
                         Osteolysis involving bones of the feet(HPO:0009134)
                            Osteolysis involving tarsal bones(HPO:0006234)
                         Abnormality of the tarsal bones(HPO:0001850)
                            Osteolysis involving tarsal bones(HPO:0006234)
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY (OMIM:259600)
Multicentric carpo-tarsal osteolysis with or without nephropathy (Orphanet:2774)
Torg-Winchester syndrome (Orphanet:3460)