Overgrowth

Symptom Information:

Symptom ID: HPO:0001548
Synonyms:
FETAL OVERGROWTH [HPO:0001548]
GENERALIZED OVERGROWTH [HPO:0001548]
Body overgrowth [Orphanet:53250]
Growth acceleration (morphologic abnormality) [Orphanet:53250]
Growth acceleration [Orphanet:53250]
Fetal overgrowth [OMIM:Fetal overgrowth]
Generalized overgrowth [OMIM:Generalized overgrowth]
Overgrowth [OMIM:Overgrowth]
Tall stature/gigantism/growth acceleration [Orphanet:53250]
Fetal overgrowth (in some patients) [OMIM:Fetal overgrowth (in some patients)]
Gigantism [MedDRA:10018265]
Gigantism (disorder) [Orphanet:53250]
Gigantism [Orphanet:53250]
Quality:
Cross references:
Orphanet:53250 "Tall stature/gigantism/growth acceleration" [Orphanet:53250]
OMIM: "Fetal overgrowth" [OMIM:Fetal overgrowth]
OMIM: "Generalized overgrowth" [OMIM:Generalized overgrowth]
OMIM: "Overgrowth" [OMIM:Overgrowth]
OMIM: "Fetal overgrowth (in some patients)" [OMIM:Fetal overgrowth (in some patients)]
UMLS:C1849265 "Overgrowth" [HPO:0001548]
UMLS:C0333957 "Growth acceleration" [Orphanet:53250]
UMLS:C0017547 "Gigantism" [Orphanet:53250]
Is a (Direct Parents):
Orphanet Tall stature
HPO         Growth abnormality
Orphanet Build/stature/longevity anomalies
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Growth abnormality(HPO:0001507)
          Overgrowth(HPO:0001548)
MedDRA:
Database Frequency: 27 / 7739
Resource:

All diseases associated with this symptom:

17q11 microdeletion syndrome (Orphanet:97685)
17q11.2 microduplication syndrome (Orphanet:139474)
48,XXYY syndrome (Orphanet:10)
Amelogenesis imperfecta - nephrocalcinosis (Orphanet:1031)
Autosomal recessive cutis laxa type 1 (Orphanet:90349)
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)
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB (OMIM:614437)
Carney complex (Orphanet:1359)
Costello syndrome (Orphanet:3071)
Dysplasia epiphysealis hemimelica (Orphanet:1822)
Dyssegmental dysplasia, Silverman-Handmaker type (Orphanet:1865)
Insulin-resistance syndrome type A (Orphanet:2297)
Linear nevus sebaceus syndrome (Orphanet:2612)
MOMO syndrome (Orphanet:2563)
Marfan syndrome type 1 (Orphanet:284963)
Megalencephaly-capillary malformation-polymicrogyria syndrome (Orphanet:60040)
Mesomelic dwarfism, Nievergelt type (Orphanet:2633)
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion (Orphanet:363700)
SCLEROSTEOSIS 1 (OMIM:269500)
SOTOS SYNDROME 2 (OMIM:614753)
Sclerosteosis (Orphanet:3152)