Asymmetric growth

Symptom Information:

Symptom ID: HPO:0100555
Synonyms:
Body asymmetry [Orphanet:53400]
Asymmetry of the body/hemiatrophy/hemihyperthrophy [Orphanet:53400]
Body asymmetry [OMIM:Body asymmetry]
Quality:
Cross references:
Orphanet:53400 "Asymmetry of the body/hemiatrophy/hemihyperthrophy" [Orphanet:53400]
OMIM: "Body asymmetry" [OMIM:Body asymmetry]
Is a (Direct Parents):
Orphanet Hemihypertrophy
HPO         Growth abnormality
Orphanet Build/stature/longevity anomalies
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Growth abnormality(HPO:0001507)
          Asymmetric growth(HPO:0100555)
MedDRA:
Database Frequency: 25 / 7739
Resource:

All diseases associated with this symptom:

1q21.1 microduplication syndrome (Orphanet:250994)
Angio-osteohypertrophic syndrome (Orphanet:2346)
Becker nevus syndrome (Orphanet:64755)
Beckwith-Wiedemann syndrome (Orphanet:116)
CHILD syndrome (Orphanet:139)
CLAPO syndrome (Orphanet:168984)
Camptodactyly - joint contractures - facial skeletal defects (Orphanet:1323)
Cutis marmorata telangiectatica congenita (Orphanet:1556)
Dysplasia epiphysealis hemimelica (Orphanet:1822)
Hemihypertrophy (Orphanet:2128)
Incontinentia pigmenti (Orphanet:464)
Ito hypomelanosis (Orphanet:435)
Linear nevus sebaceus syndrome (Orphanet:2612)
Localized scleroderma (Orphanet:90289)
Malignant hyperthermia - arthrogryposis - torticollis (Orphanet:2215)
Megalencephaly-capillary malformation-polymicrogyria syndrome (Orphanet:60040)
Non-rhizomelic chondrodysplasia punctata (Orphanet:176)
Oliver syndrome (Orphanet:2920)
Progressive hemifacial atrophy (Orphanet:1214)
Proteus syndrome (Orphanet:744)
Proteus-like syndrome (Orphanet:2969)
Silver-Russell syndrome (Orphanet:813)
Split hand - urinary anomalies - spina bifida (Orphanet:2437)
X-linked dominant chondrodysplasia, Chassaing-Lacombe type (Orphanet:163966)
X-linked mandibulofacial dysostosis (Orphanet:1131)