Proximal femoral metaphyseal irregularity
Symptom Information:
Symptom ID: | HPO:0003411 | ||
Synonyms: |
|
||
Quality: | |||
Cross references: |
|
||
Is a (Direct Parents): |
|
||
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 neck or head region(HPO:0003366) Proximal femoral metaphyseal irregularity(HPO:0003411) MedDRA: |
||
Database Frequency: | 7 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal dominant brachyolmia | (Orphanet:93304) |
Axial spondylometaphyseal dysplasia | (Orphanet:168549) |
Brachyolmia | (Orphanet:1293) |
Metaphyseal chondrodysplasia, Kaitila type | (Orphanet:166038) |
Multiple epiphyseal dysplasia, with severe proximal femoral dysplasia | (Orphanet:166029) |
Shwachman-Diamond syndrome | (Orphanet:811) |
Spondyloepimetaphyseal dysplasia - hypotrichosis | (Orphanet:168443) |