Hemihypertrophy
Symptom Information:
Symptom ID: | HPO:0001528 | ||||||||
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) Hemihypertrophy(HPO:0001528) 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) Hemihypertrophy(HPO:0001528) MedDRA: Congenital, familial and genetic disorders(MedDRA:10010331) Congenital and hereditary disorders NEC(MedDRA:10027664) Congenital disorders NEC(MedDRA:10010445) Hemihypertrophy(HPO:0001528) |
||||||||
Database Frequency: | 13 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
ANGIOKERATOMA CORPORIS DIFFUSUM WITH ARTERIOVENOUS FISTULAS | (OMIM:600419) |
Angio-osteohypertrophic syndrome | (Orphanet:2346) |
Beckwith-Wiedemann syndrome | (Orphanet:116) |
Beckwith-Wiedemann syndrome due to 11p15 microdeletion | (Orphanet:231127) |
Beckwith-Wiedemann syndrome due to CDKN1C mutation | (Orphanet:231120) |
Beckwith-Wiedemann syndrome due to NSD1 mutation | (Orphanet:238613) |
Beckwith-Wiedemann syndrome due to imprinting defect of 11p15 | (Orphanet:231117) |
Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11 | (Orphanet:96193) |
CLOVE syndrome | (Orphanet:140944) |
Hemihypertrophy | (Orphanet:2128) |
Hypoinsulinemic hypoglycemia and body hemihypertrophy | (Orphanet:293964) |
Klippel-Trénaunay syndrome | (Orphanet:90308) |
Proteus syndrome | (Orphanet:744) |