Proximal femoral metaphyseal abnormality

Symptom Information:

Symptom ID: HPO:0006431
Synonyms:
Metaphyseal abnormalities of distal and proximal femurs [OMIM:Metaphyseal abnormalities of distal and proximal femurs]
Quality:
Cross references:
OMIM: "Metaphyseal abnormalities of distal and proximal femurs" [OMIM:Metaphyseal abnormalities of distal and proximal femurs]
Is a (Direct Parents):
HPO         Abnormality of the femoral metaphysis
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 appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Abnormality of the lower limb(HPO:0002814)
                      Abnormality of the femur(HPO:0002823)
                         Abnormality of the femoral metaphysis(HPO:0006489)
                            Proximal femoral metaphyseal abnormality(HPO:0006431)
                      Abnormality of lower-limb metaphyses(HPO:0006490)
                         Abnormality of the femoral metaphysis(HPO:0006489)
                            Proximal femoral metaphyseal abnormality(HPO:0006431)
                   Abnormality of the metaphyses(HPO:0000944)
                      Abnormality of lower-limb metaphyses(HPO:0006490)
                         Abnormality of the femoral metaphysis(HPO:0006489)
                            Proximal femoral metaphyseal abnormality(HPO:0006431)
             Abnormality of long bone morphology(HPO:0011314)
                Abnormality of the metaphyses(HPO:0000944)
                   Abnormality of lower-limb metaphyses(HPO:0006490)
                      Abnormality of the femoral metaphysis(HPO:0006489)
                         Proximal femoral metaphyseal abnormality(HPO:0006431)
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Metaphyseal chondrodysplasia, Schmid type (Orphanet:174)