Hemihypertrophy

Symptom Information:

Symptom ID: HPO:0001528
Synonyms:
Asymmetric limb hypertrophy [HPO:0001528]
Body hemihypertrophy [Orphanet:53400]
Asymmetric limb hypertrophy [OMIM:Asymmetric limb hypertrophy]
Hemihypertrophy [OMIM:Hemihypertrophy]
Asymmetry of the body/hemiatrophy/hemihyperthrophy [Orphanet:53400]
Hemihypertrophy [Orphanet:53400]
Hemihypertrophy [MedDRA:10019463]
Hemihypertrophy (major feature) [OMIM:Hemihypertrophy (major feature)]
Quality:
Cross references:
Orphanet:53400 "Asymmetry of the body/hemiatrophy/hemihyperthrophy" [Orphanet:53400]
OMIM: "Asymmetric limb hypertrophy" [OMIM:Asymmetric limb hypertrophy]
OMIM: "Hemihypertrophy" [OMIM:Hemihypertrophy]
OMIM: "Hemihypertrophy (major feature)" [OMIM:Hemihypertrophy (major feature)]
UMLS:C0332890 "Hemihypertrophy" [HPO:0001528]
Is a (Direct Parents):
HPO         Abnormality of limb bone morphology
MedDRA Congenital disorders NEC
HPO         Asymmetric growth
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)
             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)