Lower limb asymmetry
Symptom Information:
Symptom ID: | HPO:0100559 | ||||||||
Synonyms: |
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Quality: | |||||||||
Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |