Asymmetric growth
Symptom Information:
Symptom ID: | HPO:0100555 | ||||||
Synonyms: |
|
||||||
Quality: | |||||||
Cross references: |
|
||||||
Is a (Direct Parents): |
|
||||||
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) |