Erlenmeyer flask deformity of the femurs
Symptom Information:
Symptom ID: | HPO:0004975 | |||||
Synonyms: |
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Is a (Direct Parents): |
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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: |
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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) |