Erlenmeyer flask deformity of the femurs

Symptom Information:

Symptom ID: HPO:0004975
Synonyms:
Erlenmeyer flask deformity of distal femur [HPO:0004975]
Erlenmeyer flask femora [HPO:0004975]
Erlenmeyer flask femora [OMIM:Erlenmeyer flask femora]
'Erlenmeyer flask' deformity of distal femur (childhood) [OMIM:'Erlenmeyer flask' deformity of distal femur (childhood)]
Erlenmeyer flask' deformity of the femurs [OMIM:Erlenmeyer flask' deformity of the femurs]
Quality:
Cross references:
OMIM: "Erlenmeyer flask femora" [OMIM:Erlenmeyer flask femora]
OMIM: "'Erlenmeyer flask' deformity of distal femur (childhood)" [OMIM:'Erlenmeyer flask' deformity of distal femur (childhood)]
OMIM: "Erlenmeyer flask' deformity of the femurs" [OMIM:Erlenmeyer flask' deformity of the femurs]
Is a (Direct Parents):
HPO         Abnormality of the femur
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)
                         Erlenmeyer flask deformity of the femurs(HPO:0004975)
MedDRA:
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

Atypical Gaucher disease due to saposin C deficiency (Orphanet:309252)
CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT (OMIM:123000)
Craniometaphyseal dysplasia (Orphanet:1522)
Gaucher disease type 1 (Orphanet:77259)
Gaucher disease type 2 (Orphanet:77260)
Gaucher disease type 3 (Orphanet:77261)
Hypertrichotic osteochondrodysplasia, Cantu type (Orphanet:1517)
Intermediate osteopetrosis (Orphanet:210110)