Hemiatrophy

Symptom Information:

Symptom ID: HPO:0100556
Synonyms:
Asymmetric limb shortening [HPO:0100556]
Hemihypotrophy [HPO:0100556]
Body hemiatrophy [Orphanet:53400]
Asymmetric limb shortening [OMIM:Asymmetric limb shortening]
Hemihypotrophy [OMIM:Hemihypotrophy]
Asymmetry of the body/hemiatrophy/hemihyperthrophy [Orphanet:53400]
Quality:
Cross references:
Orphanet:53400 "Asymmetry of the body/hemiatrophy/hemihyperthrophy" [Orphanet:53400]
OMIM: "Asymmetric limb shortening" [OMIM:Asymmetric limb shortening]
OMIM: "Hemihypotrophy" [OMIM:Hemihypotrophy]
Is a (Direct Parents):
HPO         Limb undergrowth
HPO         Asymmetric growth
Orphanet Build/stature/longevity anomalies
Orphanet Hemihypertrophy
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Growth abnormality(HPO:0001507)
          Asymmetric growth(HPO:0100555)
             Hemiatrophy(HPO:0100556)
       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)
             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)
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

HHHH SYNDROME (OMIM:306960)
X-linked dominant chondrodysplasia punctata (Orphanet:35173)