Abnormality of the abdominal wall
Symptom Information:
Symptom ID: | HPO:0004298 | |||||||
Synonyms: |
|
|||||||
Quality: | ||||||||
Cross references: |
|
|||||||
Is a (Direct Parents): |
|
|||||||
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) |