Abnormality of the abdominal wall

Symptom Information:

Symptom ID: HPO:0004298
Synonyms:
Abnormality of external features of the abdomen [HPO:0004298]
Abdominal wall anomaly [Orphanet:17000]
Congenital anomaly of abdominal wall (disorder) [Orphanet:17000]
Congenital anomaly of abdominal wall [Orphanet:17000]
Anomalies of the abdominal wall [Orphanet:17000]
Abdominal wall anomaly [MedDRA:10000101]
Anomalies of abdominal wall, congenital [MedDRA:10000101]
Quality:
Cross references:
Orphanet:17000 "Anomalies of the abdominal wall" [Orphanet:17000]
UMLS:C0009680 "Congenital anomaly of abdominal wall" [Orphanet:17000]
Is a (Direct Parents):
MedDRA Abdominal wall conditions NEC
HPO         Abnormality of the abdomen
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)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Abdominal hernias and other abdominal wall conditions(MedDRA:10000073)
       Abdominal wall conditions NEC(MedDRA:10052777)
          Abnormality of the abdominal wall(HPO:0004298)
Database Frequency: 20 / 7739
Resource:

All diseases associated with this symptom:

Axenfeld-Rieger syndrome (Orphanet:782)
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:212750)
Cranioectodermal dysplasia (Orphanet:1515)
Desmoid tumor (Orphanet:873)
Dyssegmental dysplasia, Silverman-Handmaker type (Orphanet:1865)
Fucosidosis (Orphanet:349)
Isolated CoQ-cytochrome C reductase deficiency (Orphanet:1460)
Leprechaunism (Orphanet:508)
Malignant peritoneal mesothelioma (Orphanet:168811)
Megacystis-microcolon-intestinal hypoperistalsis syndrome (Orphanet:2241)
Mowat-Wilson syndrome (Orphanet:2152)
Peritoneal cystic mesothelioma (Orphanet:168816)
Platyspondylic dysplasia, Torrance type (Orphanet:85166)
Primary peritoneal carcinoma (Orphanet:168829)
Pseudomyxoma peritonei (Orphanet:26790)
Rabson-Mendenhall syndrome (Orphanet:769)
Reticular dysgenesis (Orphanet:33355)
Spondyloepimetaphyseal dysplasia, Shohat type (Orphanet:93352)
Syndromic X-linked ichthyosis (Orphanet:281090)
Tyrosinemia type 1 (Orphanet:882)