Tibial bowing

Symptom Information:

Symptom ID: HPO:0002982
Synonyms:
Bowed tibia [HPO:0002982]
Bowing of the tibia [HPO:0002982]
Bowed tibia [OMIM:Bowed tibia]
Bowing of the tibia [OMIM:Bowing of the tibia]
Tibial bowing [OMIM:Tibial bowing]
Bowed tibias [OMIM:Bowed tibias]
Quality:
Cross references:
OMIM: "Bowed tibia" [OMIM:Bowed tibia]
OMIM: "Bowing of the tibia" [OMIM:Bowing of the tibia]
OMIM: "Tibial bowing" [OMIM:Tibial bowing]
OMIM: "Bowed tibias" [OMIM:Bowed tibias]
Is a (Direct Parents):
HPO         Bowing of the legs
HPO         Abnormality of the tibia
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 legs(HPO:0002979)
                            Tibial bowing(HPO:0002982)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Abnormality of the lower limb(HPO:0002814)
                      Bowing of the legs(HPO:0002979)
                         Tibial bowing(HPO:0002982)
                      Abnormality of the calf(HPO:0002981)
                         Abnormality of the tibia(HPO:0002992)
                            Tibial bowing(HPO:0002982)
                   Anomaly of the limb diaphyses(HPO:0006504)
                      Bowing of the long bones(HPO:0006487)
                         Bowing of the legs(HPO:0002979)
                            Tibial bowing(HPO:0002982)
MedDRA:
Database Frequency: 36 / 7739
Resource:

All diseases associated with this symptom:

Atelosteogenesis type I (Orphanet:1190)
Atelosteogenesis type III (Orphanet:56305)
CHST3-related skeletal dysplasia (Orphanet:263463)
Caffey disease (Orphanet:1310)
Dent disease type 1 (Orphanet:93622)
FIBULAR APLASIA, TIBIAL CAMPOMELIA, AND OLIGOSYNDACTYLY SYNDROME (OMIM:246570)
Geroderma osteodysplastica (Orphanet:2078)
Grant syndrome (Orphanet:2097)
Growth delay - hydrocephaly - lung hypoplasia (Orphanet:3035)
HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE (OMIM:300554)
Hereditary hypophosphatemic rickets with hypercalciuria (Orphanet:157215)
Hypocalcemic vitamin D-dependent rickets (Orphanet:289157)
Hypocalcemic vitamin D-resistant rickets (Orphanet:93160)
KNIEST-LIKE DYSPLASIA WITH PURSED LIPS AND ECTOPIA LENTIS (OMIM:245160)
Kyphomelic dysplasia (Orphanet:1801)
Léri-Weill dyschondrosteosis (Orphanet:240)
Metaphyseal acroscyphodysplasia (Orphanet:1240)
Metaphyseal anadysplasia (Orphanet:1040)
Microcephalic osteodysplastic primordial dwarfism type 2 (Orphanet:2637)
Microphthalmia with limb anomalies (Orphanet:1106)
OSTEOGENESIS IMPERFECTA, TYPE II (OMIM:166210)
OSTEOGENESIS IMPERFECTA, TYPE III (OMIM:259420)
OSTEOGENESIS IMPERFECTA, TYPE VIII (OMIM:610915)
OSTEOSCLEROSIS WITH ICHTHYOSIS AND FRACTURES (OMIM:166740)
Osteodysplasty, Melnick-Needles type (Orphanet:2484)
Osteogenesis imperfecta type 2 (Orphanet:216804)
Osteogenesis imperfecta type 3 (Orphanet:216812)
Otopalatodigital syndrome (Orphanet:669)
Otopalatodigital syndrome type 2 (Orphanet:90652)
Schinzel-Giedion syndrome (Orphanet:798)
Spondyloepimetaphyseal dysplasia, Missouri type (Orphanet:93356)
Spondylometaphyseal dysplasia - cone-rod dystrophy (Orphanet:85167)
Stüve-Wiedemann syndrome (Orphanet:3206)
VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B (OMIM:600081)
VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR (OMIM:600785)
X-linked hypophosphatemia (Orphanet:89936)