Peritoneal cystic mesothelioma
General Information (adopted from Orphanet):
| Synonyms, Signs: |
Benign multicystic peritoneal mesothelioma Multilocular peritoneal inclusion cyst Multicystic mesothelioma |
| Number of Symptoms | 8 |
| OrphanetNr: | 168816 |
| OMIM Id: |
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| ICD-10: |
C45.1 |
| UMLs: |
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| MeSH: |
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| MedDRA: |
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| Snomed: |
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Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
Unknown [Orphanet] |
| Age of onset: |
Adult [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Primary malignant peritoneal tumor
-Rare abdominal surgical disease -Rare oncologic disease |
Symptom Information:
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(HPO:0000858) | Menstrual irregularities | Frequent [Orphanet] | 42 / 7739 | |||
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(HPO:0000142) | Abnormality of the vagina | Frequent [Orphanet] | 24 / 7739 | |||
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(HPO:0002019) | Constipation | Very frequent [Orphanet] | 194 / 7739 | |||
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(HPO:0004298) | Abnormality of the abdominal wall | Very frequent [Orphanet] | 20 / 7739 | |||
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(HPO:0002585) | Abnormality of the peritoneum | Very frequent [Orphanet] | 9 / 7739 | |||
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(HPO:0002027) | Abdominal pain | Very frequent [Orphanet] | 184 / 7739 | |||
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(HPO:0004325) | Decreased body weight | Frequent [Orphanet] | 492 / 7739 | |||
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(HPO:0002664) | Neoplasm | Very frequent [Orphanet] | 111 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
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