Avascular necrosis of the capital femoral epiphysis

Symptom Information:

Symptom ID: HPO:0005743
Synonyms:
Coxa plana [HPO:0005743]
Legg-Calve-Perthes syndrome [HPO:0005743]
Legg-Perthes disease [HPO:0005743]
Morbus Legg-Calve-Perthes [HPO:0005743]
Osteochondrosis of the femoral head [HPO:0005743]
Perthes-like femoral head changes [HPO:0005743]
Coxa plana [Orphanet:46600]
Coxa plana (disorder) [Orphanet:46600]
Legg-Calve-Perthes Disease [Orphanet:46600]
Coxa plana [OMIM:Coxa plana]
Perthes-like femoral head changes [OMIM:Perthes-like femoral head changes]
Hip dislocation/dysplasia/coxa valga/coxa vara/coxa plana [Orphanet:46600]
Perthes' disease [Orphanet:46600]
Osteochondrosis [MedDRA:10031233]
Adult osteochondrosis of spine [MedDRA:10031233]
Calve-Perthe's disease [MedDRA:10031233]
Epiphyseal ischaemic necrosis [MedDRA:10031233]
Epiphyseal ischemic necrosis [MedDRA:10031233]
Juvenile osteochondrosis [MedDRA:10031233]
Juvenile osteochondrosis of foot [MedDRA:10031233]
Juvenile osteochondrosis of hip and pelvis [MedDRA:10031233]
Juvenile osteochondrosis of lower extremity, excluding foot [MedDRA:10031233]
Juvenile osteochondrosis of spine [MedDRA:10031233]
Juvenile osteochondrosis of upper extremity [MedDRA:10031233]
Osgood-Schlatter's disease [MedDRA:10031233]
Osteochondritis dissecans [MedDRA:10031233]
Osteochondrosis juvenilis [MedDRA:10031233]
Osteochondrosis of femoral head [MedDRA:10031233]
Osteochondrosis of foot [MedDRA:10031233]
Osteochondrosis of leg (excl hip) [MedDRA:10031233]
Osteochondrosis of tibial tubercle [MedDRA:10031233]
Osteochondrosis of upper limb [MedDRA:10031233]
Other juvenile osteochondrosis [MedDRA:10031233]
Perthes' disease [MedDRA:10031233]
Scheuermann's disease [MedDRA:10031233]
Schuermann's disease [MedDRA:10031233]
Freiberg's disease [MedDRA:10031233]
Sinding-Larsen-Johansson disease [MedDRA:10031233]
Osteochondrosis of spine [MedDRA:10031233]
Kienbock's disease [MedDRA:10031233]
Vertebral osteochondrosis [MedDRA:10031233]
Osteochondral defects [MedDRA:10031233]
Coxa plana (mid-childhood) [OMIM:Coxa plana (mid-childhood)]
Legg-Calve-Perthes disease [OMIM:Legg-Calve-Perthes disease]
Quality:
Cross references:
Orphanet:46600 "Hip dislocation/dysplasia/coxa valga/coxa vara/coxa plana" [Orphanet:46600]
OMIM: "Coxa plana" [OMIM:Coxa plana]
OMIM: "Perthes-like femoral head changes" [OMIM:Perthes-like femoral head changes]
OMIM: "Coxa plana (mid-childhood)" [OMIM:Coxa plana (mid-childhood)]
OMIM: "Legg-Calve-Perthes disease" [OMIM:Legg-Calve-Perthes disease]
UMLS:C0023234 "Legg-Calve-Perthes Disease" [Orphanet:46600]
Is a (Direct Parents):
HPO         Juvenile aseptic necrosis
Orphanet Hip dysplasia
HPO         Abnormality of the epiphysis of the femoral head
MedDRA Cartilage disorders
Orphanet Joint dislocation
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal physiology(HPO:0011843)
             Aseptic necrosis(HPO:0010885)
                Juvenile aseptic necrosis(HPO:0100323)
                   Avascular necrosis of the capital femoral epiphysis(HPO:0005743)
          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 lower limb epiphysis morphology(HPO:0006500)
                         Abnormality of femoral epiphysis(HPO:0006499)
                            Abnormality of the epiphysis of the femoral head(HPO:0010574)
                               Avascular necrosis of the capital femoral epiphysis(HPO:0005743)
                      Abnormality of the femur(HPO:0002823)
                         Abnormality of femoral epiphysis(HPO:0006499)
                            Abnormality of the epiphysis of the femoral head(HPO:0010574)
                               Avascular necrosis of the capital femoral epiphysis(HPO:0005743)
                         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)
                                  Avascular necrosis of the capital femoral epiphysis(HPO:0005743)
                   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)
                               Avascular necrosis of the capital femoral epiphysis(HPO:0005743)
             Abnormality of long bone morphology(HPO:0011314)
                Abnormality of epiphysis morphology(HPO:0005930)
                   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)
                               Avascular necrosis of the capital femoral epiphysis(HPO:0005743)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Tendon, ligament and cartilage disorders(MedDRA:10043237)
       Cartilage disorders(MedDRA:10007709)
          Avascular necrosis of the capital femoral epiphysis(HPO:0005743)
Database Frequency: 17 / 7739
Resource:

All diseases associated with this symptom:

48,XXYY syndrome (Orphanet:10)
DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED (OMIM:304950)
Familial avascular necrosis of femoral head (Orphanet:86820)
Gaucher disease type 1 (Orphanet:77259)
Gaucher disease type 2 (Orphanet:77260)
Gaucher disease type 3 (Orphanet:77261)
Hip dysplasia, Beukes type (Orphanet:2114)
Langer-Giedion syndrome (Orphanet:502)
Legg-Calvé-Perthes disease (Orphanet:2380)
Multiple epiphyseal dysplasia type 1 (Orphanet:93308)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
Spondyloepiphyseal dysplasia tarda (Orphanet:93284)
Steinert myotonic dystrophy (Orphanet:273)
TRICHORHINOPHALANGEAL SYNDROME, TYPE I (OMIM:190350)
TRICHORHINOPHALANGEAL SYNDROME, TYPE III (OMIM:190351)
Trichorhinophalangeal syndrome type 1 and 3 (Orphanet:77258)
Wolcott-Rallison syndrome (Orphanet:1667)