Overgrowth
Symptom Information:
Symptom ID: | HPO:0001548 | |||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Growth abnormality(HPO:0001507) Overgrowth(HPO:0001548) MedDRA: |
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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) |