Abdominal wall defect

Symptom Information:

Symptom ID: HPO:0010866
Synonyms:
Congenital anterior abdominal wall defect [HPO:0010866]
Quality:
Cross references:
Is a (Direct Parents):
HPO         Abnormality of the abdominal wall
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal wall(HPO:0004298)
             Abdominal wall defect(HPO:0010866)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Beckwith-Wiedemann syndrome due to 11p15 microdeletion (Orphanet:231127)
Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion (Orphanet:231130)
Beckwith-Wiedemann syndrome due to CDKN1C mutation (Orphanet:231120)
Beckwith-Wiedemann syndrome due to imprinting defect of 11p15 (Orphanet:231117)
Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11 (Orphanet:96193)