Hypoplasia of the capital femoral epiphysis

Symptom Information:

Symptom ID: HPO:0003090
Synonyms:
Small capital femoral epiphyses [HPO:0003090]
Small femoral capital epiphyses [HPO:0003090]
Small proximal femoral epiphyses [HPO:0003090]
Small capital femoral epiphyses [OMIM:Small capital femoral epiphyses]
Small femoral capital epiphyses [OMIM:Small femoral capital epiphyses]
Small proximal femoral epiphyses [OMIM:Small proximal femoral epiphyses]
Quality:
Cross references:
OMIM: "Small capital femoral epiphyses" [OMIM:Small capital femoral epiphyses]
OMIM: "Small femoral capital epiphyses" [OMIM:Small femoral capital epiphyses]
OMIM: "Small proximal femoral epiphyses" [OMIM:Small proximal femoral epiphyses]
Is a (Direct Parents):
HPO         Aplasia/Hypoplasia of the capital femoral epiphysis
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 head(HPO:0003368)
                               Abnormality of the epiphysis of the femoral head(HPO:0010574)
                                  Aplasia/Hypoplasia of the capital femoral epiphysis(HPO:0005003)
                                     Hypoplasia of the capital femoral epiphysis(HPO:0003090)
                         Abnormality of femoral epiphysis(HPO:0006499)
                            Abnormality of the epiphysis of the femoral head(HPO:0010574)
                               Aplasia/Hypoplasia of the capital femoral epiphysis(HPO:0005003)
                                  Hypoplasia of the capital femoral epiphysis(HPO:0003090)
                      Abnormality of lower limb epiphysis morphology(HPO:0006500)
                         Abnormality of femoral epiphysis(HPO:0006499)
                            Abnormality of the epiphysis of the femoral head(HPO:0010574)
                               Aplasia/Hypoplasia of the capital femoral epiphysis(HPO:0005003)
                                  Hypoplasia of the capital femoral epiphysis(HPO:0003090)
                   Abnormality of limb epiphysis morphology(HPO:0006505)
                      Abnormality of lower limb epiphysis morphology(HPO:0006500)
                         Abnormality of femoral epiphysis(HPO:0006499)
                            Abnormality of the epiphysis of the femoral head(HPO:0010574)
                               Aplasia/Hypoplasia of the capital femoral epiphysis(HPO:0005003)
                                  Hypoplasia of the capital femoral epiphysis(HPO:0003090)
             Abnormality of long bone morphology(HPO:0011314)
                Abnormality of epiphysis morphology(HPO:0005930)
                   Absent epiphyses(HPO:0010577)
                      Aplasia/Hypoplasia of the capital femoral epiphysis(HPO:0005003)
                         Hypoplasia of the capital femoral epiphysis(HPO:0003090)
                   Abnormality of limb epiphysis morphology(HPO:0006505)
                      Abnormality of lower limb epiphysis morphology(HPO:0006500)
                         Abnormality of femoral epiphysis(HPO:0006499)
                            Abnormality of the epiphysis of the femoral head(HPO:0010574)
                               Aplasia/Hypoplasia of the capital femoral epiphysis(HPO:0005003)
                                  Hypoplasia of the capital femoral epiphysis(HPO:0003090)
MedDRA:
Database Frequency: 15 / 7739
Resource:

All diseases associated with this symptom:

CHST3-related skeletal dysplasia (Orphanet:263463)
Connective tissue disorder due to lysyl hydroxylase-3 deficiency (Orphanet:300284)
Geleophysic dysplasia (Orphanet:2623)
MEIER-GORLIN SYNDROME 5 (OMIM:613805)
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III (OMIM:210730)
Multiple epiphyseal dysplasia type 5 (Orphanet:93311)
Multiple epiphyseal dysplasia, Lowry type (Orphanet:166016)
Roifman syndrome (Orphanet:353298)
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED (OMIM:313400)
Saldino-Mainzer syndrome (Orphanet:140969)
Schimke immuno-osseous dysplasia (Orphanet:1830)
Spondyloepimetaphyseal dysplasia with multiple dislocations (Orphanet:93360)
Spondyloepiphyseal dysplasia, MacDermot type (Orphanet:163668)
Spondyloepiphyseal dysplasia, Reardon type (Orphanet:163662)
Spondylometaphyseal dysplasia, A4 type (Orphanet:168555)