Broad femoral neck

Symptom Information:

Symptom ID: HPO:0006429
Synonyms:
Broadening of femoral neck [HPO:0006429]
Wide femoral neck [HPO:0006429]
Widened femoral necks [HPO:0006429]
Broad femoral neck [OMIM:Broad femoral neck]
Wide femoral neck [OMIM:Wide femoral neck]
Widened femoral necks [OMIM:Widened femoral necks]
Broadening of femoral neck (mid-childhood) [OMIM:Broadening of femoral neck (mid-childhood)]
Widened femoral neck [OMIM:Widened femoral neck]
Quality:
Cross references:
OMIM: "Broad femoral neck" [OMIM:Broad femoral neck]
OMIM: "Wide femoral neck" [OMIM:Wide femoral neck]
OMIM: "Widened femoral necks" [OMIM:Widened femoral necks]
OMIM: "Broadening of femoral neck (mid-childhood)" [OMIM:Broadening of femoral neck (mid-childhood)]
OMIM: "Widened femoral neck" [OMIM:Widened femoral neck]
Is a (Direct Parents):
HPO         Abnormality of the femoral neck
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:
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)