Lower limb asymmetry

Symptom Information:

Symptom ID: HPO:0100559
Synonyms:
Leg length discrepancy [HPO:0100559]
Leg length discrepancy [OMIM:Leg length discrepancy]
Lower limb asymmetry [OMIM:Lower limb asymmetry]
Lower limb asymmetry/hemiatrophy/hemihypertrophy [Orphanet:21320]
Leg length discrepancy (in some patients) [OMIM:Leg length discrepancy (in some patients)]
Quality:
Cross references:
Orphanet:21320 "Lower limb asymmetry/hemiatrophy/hemihypertrophy" [Orphanet:21320]
OMIM: "Leg length discrepancy" [OMIM:Leg length discrepancy]
OMIM: "Lower limb asymmetry" [OMIM:Lower limb asymmetry]
OMIM: "Leg length discrepancy (in some patients)" [OMIM:Leg length discrepancy (in some patients)]
Is a (Direct Parents):
HPO         Abnormality of the lower limb
Orphanet Abnormality of the lower limb
HPO         Asymmetric growth
Orphanet Hemihypertrophy of lower limb
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)
                      Lower limb asymmetry(HPO:0100559)
       Growth abnormality(HPO:0001507)
          Asymmetric growth(HPO:0100555)
             Lower limb asymmetry(HPO:0100559)
MedDRA:
Database Frequency: 30 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
Angio-osteohypertrophic syndrome (Orphanet:2346)
CLAPO syndrome (Orphanet:168984)
CLOVE syndrome (Orphanet:140944)
Cleft lip/palate - deafness - sacral lipoma (Orphanet:2003)
Currarino triad (Orphanet:1552)
Dysspondyloenchondromatosis (Orphanet:85198)
Familial multiple nevi flammei (Orphanet:624)
Focal dermal hypoplasia (Orphanet:2092)
Hennekam-Beemer syndrome (Orphanet:2135)
Intellectual deficit - hypotonia - skin hyperpigmentation (Orphanet:3050)
Klippel-Trénaunay syndrome (Orphanet:90308)
Limb body wall complex (Orphanet:2369)
Localized scleroderma (Orphanet:90289)
Lower limb deficiency - hypospadias (Orphanet:2487)
Maffucci syndrome (Orphanet:163634)
Melorheostosis (Orphanet:2485)
Mosaic trisomy 14 (Orphanet:1703)
Multiple benign circumferential skin creases on limbs (Orphanet:2505)
Parastremmatic dwarfism (Orphanet:2646)
Parkes Weber syndrome (Orphanet:90307)
Proteus syndrome (Orphanet:744)
Proteus-like syndrome (Orphanet:2969)
Rombo syndrome (Orphanet:3110)
Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus (Orphanet:137608)
Splenogonadal fusion - limb defects - micrognathia (Orphanet:2063)
Spondylometaphyseal dysplasia, 'corner fracture' type (Orphanet:93315)
Toriello-Lacassie-Droste syndrome (Orphanet:3339)
Townes-Brocks syndrome (Orphanet:857)
Ulnar/fibula ray defect - brachydactyly (Orphanet:52056)