Broad femoral neck
Symptom Information:
Symptom ID: | HPO:0006429 | ||||||||
Synonyms: |
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Quality: | |||||||||
Cross references: |
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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) Abnormality of the femoral neck or head region(HPO:0003366) Abnormality of the femoral neck(HPO:0003367) Broad femoral neck(HPO:0006429) MedDRA: |
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Database Frequency: | 18 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III | (OMIM:611929) |
Costello syndrome | (Orphanet:3071) |
Desbuquois syndrome | (Orphanet:1425) |
Dysosteosclerosis | (Orphanet:1782) |
Ehlers-Danlos syndrome, spondylocheirodysplastic type | (Orphanet:157965) |
Fibrodysplasia ossificans progressiva | (Orphanet:337) |
Hip dysplasia, Beukes type | (Orphanet:2114) |
Hurler syndrome | (Orphanet:93473) |
Multiple epiphyseal dysplasia type 1 | (Orphanet:93308) |
Multiple epiphyseal dysplasia type 5 | (Orphanet:93311) |
Multiple epiphyseal dysplasia, with miniepiphyses | (Orphanet:166032) |
Multiple epiphyseal dysplasia, with severe proximal femoral dysplasia | (Orphanet:166029) |
Roifman syndrome | (Orphanet:353298) |
SMITH-MCCORT DYSPLASIA 2 | (OMIM:615222) |
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE, LEROY-SPRANGERTYPE | (OMIM:609223) |
Spondyloepimetaphyseal dysplasia - abnormal dentition | (Orphanet:168451) |
Spondyloepimetaphyseal dysplasia, Irapa type | (Orphanet:93351) |
Upington disease | (Orphanet:3408) |