Radial bowing

Symptom Information:

Symptom ID: HPO:0002986
Synonyms:
Bowed radii [HPO:0002986]
Bowed radius [HPO:0002986]
Bowed radii [OMIM:Bowed radii]
Bowed radius [OMIM:Bowed radius]
Radial bowing [OMIM:Radial bowing]
Quality:
Cross references:
OMIM: "Bowed radii" [OMIM:Bowed radii]
OMIM: "Bowed radius" [OMIM:Bowed radius]
OMIM: "Radial bowing" [OMIM:Radial bowing]
Is a (Direct Parents):
HPO         Abnormality of the radius
HPO         Bowed forearm bones
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)
             Abnormality of long bone morphology(HPO:0011314)
                Abnormal diaphysis morphology(HPO:0000940)
                   Anomaly of the limb diaphyses(HPO:0006504)
                      Bowing of the long bones(HPO:0006487)
                         Bowing of the arm(HPO:0006488)
                            Bowed forearm bones(HPO:0003956)
                               Radial bowing(HPO:0002986)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Anomaly of the limb diaphyses(HPO:0006504)
                      Bowing of the long bones(HPO:0006487)
                         Bowing of the arm(HPO:0006488)
                            Bowed forearm bones(HPO:0003956)
                               Radial bowing(HPO:0002986)
                   Abnormality of the upper limb(HPO:0002817)
                      Abnormality of the forearm(HPO:0002973)
                         Bowed forearm bones(HPO:0003956)
                            Radial bowing(HPO:0002986)
                         Abnormality of the radius(HPO:0002818)
                            Radial bowing(HPO:0002986)
                      Bowing of the arm(HPO:0006488)
                         Bowed forearm bones(HPO:0003956)
                            Radial bowing(HPO:0002986)
MedDRA:
Database Frequency: 27 / 7739
Resource:

All diseases associated with this symptom:

Absent tibia - polydactyly - arachnoid cyst (Orphanet:3328)
Acromesomelic dysplasia, Hunter-Thomson type (Orphanet:968)
Acromesomelic dysplasia, Maroteaux type (Orphanet:40)
Atelosteogenesis type I (Orphanet:1190)
Atelosteogenesis type III (Orphanet:56305)
Dyschondrosteosis - nephritis (Orphanet:1765)
Fuhrmann syndrome (Orphanet:2854)
HYPOPROTEINEMIA, HYPERCATABOLIC (OMIM:241600)
Kyphomelic dysplasia (Orphanet:1801)
Langer mesomelic dysplasia (Orphanet:2632)
Léri-Weill dyschondrosteosis (Orphanet:240)
MESOMELIC DYSPLASIA, KANTAPUTRA TYPE (OMIM:156232)
Marshall syndrome (Orphanet:560)
Mesomelic dysplasia, Kantaputra type (Orphanet:1836)
Metaphyseal anadysplasia (Orphanet:1040)
Microcephalic osteodysplastic primordial dwarfism type 2 (Orphanet:2637)
OSTEOGENESIS IMPERFECTA, TYPE VIII (OMIM:610915)
Ophthalmomandibulomelic dysplasia (Orphanet:2741)
Otopalatodigital syndrome (Orphanet:669)
Otopalatodigital syndrome type 2 (Orphanet:90652)
Phocomelia, Schinzel type (Orphanet:2879)
Postaxial tetramelic oligodactyly (Orphanet:2730)
Radio-ulnar synostosis - amegakaryocytic thrombocytopenia (Orphanet:71289)
Spondyloepimetaphyseal dysplasia with joint laxity (Orphanet:93359)
Spondyloepimetaphyseal dysplasia, Missouri type (Orphanet:93356)
Upper limb mesomelic dysplasia (Orphanet:2497)
W syndrome (Orphanet:2804)