Ascites

Symptom Information:

Symptom ID: HPO:0001541
Synonyms:
Ascitis [Orphanet:26860]
Ascites [OMIM:Ascites]
Ascites (in some patients) [OMIM:Ascites (in some patients)]
Ascites [MedDRA:10003445]
Quality:
Cross references:
Orphanet:26860 "Ascitis" [Orphanet:26860]
OMIM: "Ascites" [OMIM:Ascites]
OMIM: "Ascites (in some patients)" [OMIM:Ascites (in some patients)]
UMLS:C0003962 "Ascites" [HPO:0001541]
Is a (Direct Parents):
HPO         Abnormality of the abdominal organs
MedDRA Peritoneal and retroperitoneal disorders
Orphanet Structural anomalies of the digestive tract
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)
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)