Hemihypotrophy of lower limb

Symptom Information:

Symptom ID: HPO:0200053
Synonyms:
Asymmetric leg shortening [HPO:0200053]
Asymmetric lower limb shortness [HPO:0200053]
Lower limb hemihypertrophy [Orphanet:21320]
Lower limb hemihypotrophy [Orphanet:21320]
Asymmetric leg shortening [OMIM:Asymmetric leg shortening]
Asymmetric lower limb shortness [OMIM:Asymmetric lower limb shortness]
Lower limb asymmetry/hemiatrophy/hemihypertrophy [Orphanet:21320]
Quality:
Cross references:
HPO:0100553 "Hemihypertrophy of lower limb" [Orphanet:21320]
Orphanet:21320 "Lower limb asymmetry/hemiatrophy/hemihypertrophy" [Orphanet:21320]
OMIM: "Asymmetric leg shortening" [OMIM:Asymmetric leg shortening]
OMIM: "Asymmetric lower limb shortness" [OMIM:Asymmetric lower limb shortness]
Is a (Direct Parents):
HPO         Hemiatrophy
Orphanet Hemihypertrophy of lower limb
Orphanet Abnormality of the lower limb
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Growth abnormality(HPO:0001507)
          Asymmetric growth(HPO:0100555)
             Hemiatrophy(HPO:0100556)
                Hemihypotrophy of lower limb(HPO:0200053)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Aplasia/hypoplasia involving the skeleton(HPO:0009115)
                Aplasia/hypoplasia of the extremities(HPO:0009815)
                   Limb undergrowth(HPO:0009826)
                      Hemiatrophy(HPO:0100556)
                         Hemihypotrophy of lower limb(HPO:0200053)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Aplasia/hypoplasia of the extremities(HPO:0009815)
                      Limb undergrowth(HPO:0009826)
                         Hemiatrophy(HPO:0100556)
                            Hemihypotrophy of lower limb(HPO:0200053)
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

ASYMMETRIC SHORT STATURE SYNDROME (OMIM:108450)
Craniofrontonasal dysplasia (Orphanet:1520)