Pseudomyxoma peritonei

General Information (adopted from Orphanet):

Synonyms, Signs: PMP
Adenomucinosis
Gelatinous ascites
Number of Symptoms 19
OrphanetNr: 26790
OMIM Id:
ICD-10: C78.6
UMLs: C0033822
MeSH: D011553
MedDRA: 10037138
Snomed: 112679004
307601000

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 peritoneal tumor
 -Rare abdominal surgical disease
 -Rare oncologic disease

Symptom Information: Sort by abundance 

1
 (HPO:0011037) Decreased urine output Occasional [Orphanet] 47 / 7739
2
 (HPO:0100615) Ovarian neoplasm Occasional [Orphanet] 25 / 7739
3
 (HPO:0002037) Inflammation of the large intestine Frequent [Orphanet] 25 / 7739
4
 (HPO:0100273) Neoplasm of the colon Occasional [Orphanet] 18 / 7739
5
 (HPO:0004298) Abnormality of the abdominal wall Very frequent [Orphanet] 20 / 7739
6
 (HPO:0005214) Intestinal obstruction Occasional [Orphanet] 35 / 7739
7
 (HPO:0002894) Neoplasm of the pancreas Occasional [Orphanet] 17 / 7739
8
 (HPO:0001541) Ascites Very frequent [Orphanet] 94 / 7739
9
 (HPO:0002585) Abnormality of the peritoneum Very frequent [Orphanet] 9 / 7739
10
 (HPO:0004299) Hernia of the abdominal wall Occasional [Orphanet] 176 / 7739
11
 (HPO:0002019) Constipation Occasional [Orphanet] 194 / 7739
12
 (HPO:0007378) Neoplasm of the gastrointestinal tract Occasional [Orphanet] 11 / 7739
13
 (HPO:0006753) Neoplasm of the stomach Occasional [Orphanet] 13 / 7739
14
 (HPO:0002027) Abdominal pain Occasional [Orphanet] 184 / 7739
15
 (HPO:0002017) Nausea and vomiting Occasional [Orphanet] 134 / 7739
16
 (HPO:0004325) Decreased body weight Occasional [Orphanet] 492 / 7739
17
 (HPO:0002093) Respiratory insufficiency Occasional [Orphanet] 410 / 7739
18
 (HPO:0002716) Lymphadenopathy Occasional [Orphanet] 129 / 7739
19
 (HPO:0001522) Death in infancy Occasional [Orphanet] 275 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: