Ascites
Symptom Information:
Symptom ID: | HPO:0001541 | ||||||
Synonyms: |
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Quality: | |||||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the abdomen(HPO:0001438) Abnormality of the abdominal organs(HPO:0002012) Ascites(HPO:0001541) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Peritoneal and retroperitoneal conditions(MedDRA:10034652) Peritoneal and retroperitoneal disorders(MedDRA:10034653) Ascites(HPO:0001541) |
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Database Frequency: | 94 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
ATTRV122I amyloidosis | (Orphanet:85451) |
Acrocephalopolydactyly | (Orphanet:221054) |
Adams-Oliver syndrome | (Orphanet:974) |
Alpha heavy-chain disease | (Orphanet:100025) |
Alström syndrome | (Orphanet:64) |
Alveolar echinococcosis | (Orphanet:284) |
Anisakiasis | (Orphanet:1070) |
Budd-Chiari syndrome | (Orphanet:131) |
Carney triad | (Orphanet:139411) |
Castleman disease | (Orphanet:160) |
Choreoacanthocytosis | (Orphanet:2388) |
Chylous ascites | (Orphanet:1160) |
Cirrhotic cardiomyopathy | (Orphanet:57777) |
Congenital disorder of glycosylation | (Orphanet:137) |
Congenital pulmonary lymphangiectasia | (Orphanet:2414) |
Congenital toxoplasmosis | (Orphanet:858) |
Cutis marmorata telangiectatica congenita | (Orphanet:1556) |
Dengue fever | (Orphanet:99828) |
Desmoplastic small round cell tumor | (Orphanet:83469) |
Diffuse neonatal hemangiomatosis | (Orphanet:2123) |
Distomatosis | (Orphanet:1685) |
ENTEROPATHY, PROTEIN-LOSING | (OMIM:226300) |
Familial Mediterranean fever | (Orphanet:342) |
Familial isolated restrictive cardiomyopathy | (Orphanet:75249) |
Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease | (Orphanet:439854) |
Fetal Gaucher disease | (Orphanet:85212) |
Fetal parvovirus syndrome | (Orphanet:295) |
Free sialic acid storage disease | (Orphanet:834) |
Free sialic acid storage disease, infantile form | (Orphanet:309324) |
Galactosemia | (Orphanet:352) |
Gaucher disease type 1 | (Orphanet:77259) |
Gaucher disease type 2 | (Orphanet:77260) |
Gaucher disease type 3 | (Orphanet:77261) |
Glycogen storage disease due to glycogen branching enzyme deficiency | (Orphanet:367) |
Glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form | (Orphanet:308712) |
Glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form | (Orphanet:308684) |
Glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form | (Orphanet:308698) |
Glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form | (Orphanet:308670) |
Glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form | (Orphanet:308655) |
Glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form | (Orphanet:308638) |
Glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form | (Orphanet:308621) |
Griscelli disease | (Orphanet:381) |
HYPERVITAMINOSIS A, SUSCEPTIBILITY TO | (OMIM:240150) |
Hemochromatosis, type 1 | (OMIM:235200) |
Hemochromatosis, type 2A | (OMIM:602390) |
Hennekam syndrome | (Orphanet:2136) |
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 | (Orphanet:137681) |
Hereditary North American Indian childhood cirrhosis | (Orphanet:168583) |
Hereditary angioedema | (Orphanet:91378) |
Hereditary nonpolyposis colon cancer | (Orphanet:144) |
Hydatidosis | (Orphanet:400) |
Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
Hypocomplementemic urticarial vasculitis | (Orphanet:36412) |
Hypotonia with lactic acidemia and hyperammonemia | (Orphanet:137908) |
Idiopathic copper-associated cirrhosis | (Orphanet:209919) |
Intestinal lymphangiectasia | (Orphanet:36204) |
Isolated polycystic liver disease | (Orphanet:2924) |
Klippel-Trénaunay syndrome | (Orphanet:90308) |
LYMPHOPROLIFERATIVE SYNDROME 2 | (OMIM:615122) |
Lethal hemolytic anemia - genital anomalies | (Orphanet:1046) |
Lymphangioleiomyomatosis | (Orphanet:538) |
Malignant peritoneal mesothelioma | (Orphanet:168811) |
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
Mosaic variegated aneuploidy syndrome | (Orphanet:1052) |
Mucopolysaccharidosis type 2, severe form | (Orphanet:217085) |
Mucopolysaccharidosis type 7 | (Orphanet:584) |
Mulibrey nanism | (Orphanet:2576) |
Mullerian derivatives - lymphangiectasia - polydactyly | (Orphanet:1655) |
Neonatal hemochromatosis | (Orphanet:446) |
Neonatal intrahepatic cholestasis due to citrin deficiency | (Orphanet:247598) |
Niemann-Pick disease type C | (Orphanet:646) |
Non-histaminic angioedema | (Orphanet:658) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
Osteocraniostenosis | (Orphanet:2763) |
Ovarian hyperstimulation syndrome | (Orphanet:64739) |
Palmoplantar keratoderma-esophageal carcinoma syndrome | (Orphanet:2198) |
Perlman syndrome | (Orphanet:2849) |
Polyarteritis nodosa | (Orphanet:767) |
Primary intestinal lymphangiectasia | (Orphanet:90362) |
Pseudomyxoma peritonei | (Orphanet:26790) |
Pulmonary arterial hypertension | (Orphanet:182090) |
Reticular dysgenesis | (Orphanet:33355) |
Reynolds syndrome | (Orphanet:779) |
SPLENOPORTAL VASCULAR ANOMALIES | (OMIM:271500) |
Secondary intestinal lymphangiectasia | (Orphanet:90363) |
Short rib-polydactyly syndrome, Beemer-Langer type | (Orphanet:93268) |
Sialidosis type 1 | (Orphanet:812) |
Sialidosis type 2 | (Orphanet:87876) |
Systemic mastocytosis | (Orphanet:2467) |
Tropical endomyocardial fibrosis | (Orphanet:75565) |
Tyrosinemia type 1 | (Orphanet:882) |
Wolman disease | (Orphanet:75233) |
XFE PROGEROID SYNDROME | (OMIM:610965) |
[DEL] GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL | (OMIM:261740) |