Bowing of the legs

Symptom Information:

Symptom ID: HPO:0002979
Synonyms:
Bowed legs [HPO:0002979]
Bowed lower limbs [HPO:0002979]
Bowed legs [OMIM:Bowed legs]
Bowed lower limbs [OMIM:Bowed lower limbs]
Bowing of the legs [OMIM:Bowing of the legs]
Leg bowing [OMIM:Leg bowing]
Lower limb bowing [OMIM:Lower limb bowing]
Quality:
Cross references:
OMIM: "Bowed legs" [OMIM:Bowed legs]
OMIM: "Bowed lower limbs" [OMIM:Bowed lower limbs]
OMIM: "Bowing of the legs" [OMIM:Bowing of the legs]
OMIM: "Leg bowing" [OMIM:Leg bowing]
OMIM: "Lower limb bowing" [OMIM:Lower limb bowing]
Is a (Direct Parents):
HPO         Abnormality of the lower limb
HPO         Bowing of the long 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 legs(HPO:0002979)
             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 legs(HPO:0002979)
                   Abnormality of the lower limb(HPO:0002814)
                      Bowing of the legs(HPO:0002979)
MedDRA:
Database Frequency: 28 / 7739
Resource:

All diseases associated with this symptom:

Childhood-onset hypophosphatasia (Orphanet:247667)
Craniometadiaphyseal dysplasia, wormian bone type (Orphanet:85184)
Cutis marmorata telangiectatica congenita (Orphanet:1556)
Dent disease type 1 (Orphanet:93622)
Diaphyseal medullary stenosis - bone malignancy (Orphanet:85182)
FANCONI RENOTUBULAR SYNDROME 3 (OMIM:615605)
Gnathodiaphyseal dysplasia (Orphanet:53697)
HYPOPHOSPHATEMIC BONE DISEASE (OMIM:146350)
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)
Hypophosphatemic rickets, autosomal recessive, 2 (OMIM:613312)
METAPHYSEAL ANADYSPLASIA 2 (OMIM:613073)
Mesomelic dwarfism - cleft palate - camptodactyly (Orphanet:2631)
Metaphyseal dysostosis - intellectual deficit - conductive deafness (Orphanet:2502)
OSTEOGENESIS IMPERFECTA, TYPE VII (OMIM:610682)
Perinatal lethal hypophosphatasia (Orphanet:247623)
Short rib-polydactyly syndrome, Beemer-Langer type (Orphanet:93268)
Spondyloepimetaphyseal dysplasia - short limb - abnormal calcification (Orphanet:93358)
Spondyloepimetaphyseal dysplasia, Pakistani type (Orphanet:93282)
Spondyloepimetaphyseal dysplasia, matrilin-3 type (Orphanet:156728)
TIBIAL TORSION, BILATERAL MEDIAL (OMIM:188800)
VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A (OMIM:264700)
VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B (OMIM:600081)
VITAMIN D-DEPENDENT RICKETS, TYPE 2A (OMIM:277440)
VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR (OMIM:600785)
X-linked hypophosphatemia (Orphanet:89936)