Short femoral neck

Symptom Information:

Symptom ID: HPO:0100864
Synonyms:
Hypoplasia of the femoral neck [HPO:0100864]
Hypoplastic femoral neck [HPO:0100864]
Short femoral necks [HPO:0100864]
Short femoral neck [OMIM:Short femoral neck]
Short femoral necks [OMIM:Short femoral necks]
short femoral neck [OMIM:short femoral neck]
Femoral neck, short [OMIM:Femoral neck, short]
Quality:
Cross references:
OMIM: "Short femoral neck" [OMIM:Short femoral neck]
OMIM: "Short femoral necks" [OMIM:Short femoral necks]
OMIM: "short femoral neck" [OMIM:short femoral neck]
OMIM: "Femoral neck, short" [OMIM:Femoral neck, short]
Is a (Direct Parents):
HPO         Abnormality of the femoral neck
HPO         Aplasia/Hypoplasia involving the femoral head and 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 pelvic girdle bone morphology(HPO:0002644)
                   Aplasia/Hypoplasia involving the pelvis(HPO:0009103)
                      Aplasia/Hypoplasia involving the femoral head and neck(HPO:0009108)
                         Short femoral neck(HPO:0100864)
                Abnormality of limb bone morphology(HPO:0002813)
                   Abnormality of the lower limb(HPO:0002814)
                      Aplasia/hypoplasia involving bones of the lower limbs(HPO:0006493)
                         Aplasia/hypoplasia of the femur(HPO:0005613)
                            Aplasia/Hypoplasia involving the femoral head and neck(HPO:0009108)
                               Short femoral neck(HPO:0100864)
                      Abnormality of the femur(HPO:0002823)
                         Abnormality of the femoral neck or head region(HPO:0003366)
                            Abnormality of the femoral neck(HPO:0003367)
                               Short femoral neck(HPO:0100864)
                            Aplasia/Hypoplasia involving the femoral head and neck(HPO:0009108)
                               Short femoral neck(HPO:0100864)
                         Aplasia/hypoplasia of the femur(HPO:0005613)
                            Aplasia/Hypoplasia involving the femoral head and neck(HPO:0009108)
                               Short femoral neck(HPO:0100864)
                   Aplasia/hypoplasia of the extremities(HPO:0009815)
                      Aplasia/hypoplasia involving bones of the lower limbs(HPO:0006493)
                         Aplasia/hypoplasia of the femur(HPO:0005613)
                            Aplasia/Hypoplasia involving the femoral head and neck(HPO:0009108)
                               Short femoral neck(HPO:0100864)
             Aplasia/hypoplasia involving the skeleton(HPO:0009115)
                Aplasia/hypoplasia of the extremities(HPO:0009815)
                   Aplasia/hypoplasia involving bones of the lower limbs(HPO:0006493)
                      Aplasia/hypoplasia of the femur(HPO:0005613)
                         Aplasia/Hypoplasia involving the femoral head and neck(HPO:0009108)
                            Short femoral neck(HPO:0100864)
MedDRA:
Database Frequency: 36 / 7739
Resource:

All diseases associated with this symptom:

Achondroplasia (Orphanet:15)
Acrocapitofemoral dysplasia (Orphanet:63446)
Autosomal dominant brachyolmia (Orphanet:93304)
Axial spondylometaphyseal dysplasia (Orphanet:168549)
BARATELA-SCOTT SYNDROME (OMIM:300881)
Brachyolmia (Orphanet:1293)
Brachyolmia type 1, Hobaek type (Orphanet:93301)
Brachyolmia type 1, Toledo type (Orphanet:93303)
CHONDRODYSPLASIA, ACROMESOMELIC, WITH GENITAL ANOMALIES (OMIM:609441)
CHST3-related skeletal dysplasia (Orphanet:263463)
Camptodactyly syndrome, Guadalajara type 1 (Orphanet:1327)
Cleidocranial dysplasia (Orphanet:1452)
Coats plus syndrome (Orphanet:313838)
Czech dysplasia, metatarsal type (Orphanet:137678)
DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED (OMIM:304950)
Desbuquois syndrome (Orphanet:1425)
Ehlers-Danlos syndrome, spondylocheirodysplastic type (Orphanet:157965)
Langer mesomelic dysplasia (Orphanet:2632)
Lipodystrophy - intellectual deficit - deafness (Orphanet:50811)
METAPHYSEAL ANADYSPLASIA 2 (OMIM:613073)
Multiple epiphyseal dysplasia type 1 (Orphanet:93308)
Multiple epiphyseal dysplasia type 5 (Orphanet:93311)
Multiple epiphyseal dysplasia, Lowry type (Orphanet:166016)
Multiple epiphyseal dysplasia, with miniepiphyses (Orphanet:166032)
Multiple epiphyseal dysplasia, with severe proximal femoral dysplasia (Orphanet:166029)
RHIZOMELIC DYSPLASIA, SCOLIOSIS, AND RETINITIS PIGMENTOSA (OMIM:610319)
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED (OMIM:313400)
Saldino-Mainzer syndrome (Orphanet:140969)
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome (Orphanet:314394)
Spondyloepimetaphyseal dysplasia - abnormal dentition (Orphanet:168451)
Spondyloepimetaphyseal dysplasia - hypotrichosis (Orphanet:168443)
Spondyloepimetaphyseal dysplasia with joint laxity (Orphanet:93359)
Spondyloepimetaphyseal dysplasia, Bieganski type (Orphanet:168448)
Spondyloepimetaphyseal dysplasia, Geneviève type (Orphanet:168454)
Spondyloepimetaphyseal dysplasia, Shohat type (Orphanet:93352)
Spondylometaphyseal dysplasia, 'corner fracture' type (Orphanet:93315)