Foot acroosteolysis

Symptom Information:

Symptom ID: HPO:0001842
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
HPO         Osteolysis involving bones of the feet
HPO         Osteolytic defects of the phalanges of the toes
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)
                         Foot acroosteolysis(HPO:0001842)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Abnormality of digit(HPO:0011297)
                      Abnormality of toe(HPO:0001780)
                         Abnormality of the phalanges of the toes(HPO:0010161)
                            Osteolytic defects of the phalanges of the toes(HPO:0010177)
                               Foot acroosteolysis(HPO:0001842)
                   Abnormality of the lower limb(HPO:0002814)
                      Abnormality of the foot(HPO:0001760)
                         Abnormality of toe(HPO:0001780)
                            Abnormality of the phalanges of the toes(HPO:0010161)
                               Osteolytic defects of the phalanges of the toes(HPO:0010177)
                                  Foot acroosteolysis(HPO:0001842)
                         Osteolysis involving bones of the feet(HPO:0009134)
                            Foot acroosteolysis(HPO:0001842)
                      Osteolysis involving bones of the lower limbs(HPO:0009139)
                         Osteolysis involving bones of the feet(HPO:0009134)
                            Foot acroosteolysis(HPO:0001842)
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Ehlers-Danlos syndrome, vascular type (Orphanet:286)
HAJDU-CHENEY SYNDROME (OMIM:102500)
Hereditary sensory and autonomic neuropathy type 2 (Orphanet:970)
Necrotizing encephalomyelopathy, subacute, of Leigh, adult (OMIM:161700)