Hemihypertrophy of lower limb

Symptom Information:

Symptom ID: HPO:0100553
Synonyms:
Lower limb hemihypertrophy [Orphanet:21320]
Lower limb asymmetry/hemiatrophy/hemihypertrophy [Orphanet:21320]
Quality:
Cross references:
HPO:0200053 "Hemihypotrophy of lower limb" [Orphanet:21320]
Orphanet:21320 "Lower limb asymmetry/hemiatrophy/hemihypertrophy" [Orphanet:21320]
Is a (Direct Parents):
HPO         Lower limb asymmetry
HPO         Hemihypertrophy
Orphanet Abnormality of the 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)
                         Hemihypertrophy of lower limb(HPO:0100553)
                   Hemihypertrophy(HPO:0001528)
                      Hemihypertrophy of lower limb(HPO:0100553)
       Growth abnormality(HPO:0001507)
          Asymmetric growth(HPO:0100555)
             Lower limb asymmetry(HPO:0100559)
                Hemihypertrophy of lower limb(HPO:0100553)
             Hemihypertrophy(HPO:0001528)
                Hemihypertrophy of lower limb(HPO:0100553)
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11 (Orphanet:96193)