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AlternativeMed
modern wellness · Symptom

Ascites

🩺 HPO Source
HPO Label
Ascites
HPO Definition
Accumulation of fluid in the peritoneal cavity (between the layers of the peritoneum that lines the abdomen).
HPO Curator Comment
Ascites is commonly associated with liver disease that has resulted in portal hypertension and low serum albumin levels.
🔤 Synonyms (2)
Synonyms
Accumulation of fluid in the abdomenPeritoneal effusion
🔗 Cross-References (2)
SNOMEDCT_US389026000
UMLSC0003962
🔼 Broader Terms (1)
🏥 Conditions where Ascites appears
40 · bridged via HPO ↔ OMIM
syndrome OMIM 200995
Acrocephalopolydactylous Dysplasia
ev: TAS
syndrome OMIM 203700
Alpers Syndrome (Disorder)
freq: 2/3 ev: PCS
syndrome OMIM 613658
Brain Calcification Rajab Type
freq: 1/1 ev: PCS
disease OMIM 115197
Cardiomyopathy, Familial Hypertrophic, 4, Susceptibility To
freq: 1/2 ev: PCS
syndrome OMIM 602347
Cholestasis, Progressive Familial Intrahepatic 3
freq: 1/2 ev: PCS
syndrome OMIM 617049
Cholestasis, Progressive Familial Intrahepatic, 5
freq: 1/4 onset: HP:0003577 ev: PCS
syndrome OMIM 215600
Cirrhosis, Cryptogenic
freq: 1/1 ev: PCS
syndrome OMIM 614702
Combined Oxidative Phosphorylation Deficiency 10
freq: 1/3 ev: PCS
syndrome OMIM 611719
Combined Oxidative Phosphorylation Deficiency 5
ev: TAS
syndrome OMIM 226300
Complement Hyperactivation, Angiopathic Thrombosis, And Protein-Losing Enteropathy
ev: IEA
syndrome OMIM 608104
Congenital Disorder of Glycosylation Type 1H
freq: 3/3 ev: PCS
syndrome OMIM 608776
Congenital Disorder of Glycosylation Type 1L
freq: 1/4 ev: PCS
syndrome OMIM 215600
Copper Toxicosis, Idiopathic
freq: 1/1 ev: PCS
syndrome OMIM 215600
Copper-Overload Cirrhosis
freq: 1/1 ev: PCS
syndrome OMIM 613177
Cutis Laxa With Severe Pulmonary, Gastrointestinal, And Urinary Abnormalities
freq: 1/4 ev: PCS
syndrome OMIM 618183
Diarrhea 10, Protein-Losing Enteropathy Type
freq: 1/1 ev: PCS
syndrome OMIM 215600
Endemic Tyrolean Infantile Cirrhosis
freq: 1/1 ev: PCS
syndrome OMIM 115197
Familial Hypertrophic Cardiomyopathy Type 4
freq: 1/2 ev: PCS
syndrome OMIM 603278
Focal Segmental Glomerulosclerosis 1
freq: 1/1 ev: PCS
syndrome OMIM 617667
Fraser Syndrome 3
freq: 1/3 ev: PCS
syndrome OMIM 606812
Fumarase Deficiency
freq: 1/2 ev: PCS
syndrome OMIM 606812
Fumaric Aciduria
freq: 1/2 ev: PCS
syndrome OMIM 608013
Gaucher Disease, Perinatal Lethal
ev: TAS
syndrome OMIM 261740
Glycogen Storage Disease of Heart, Lethal Congenital
freq: 1/5 ev: PCS
syndrome OMIM 232500
Glycogen Storage Disease Type Iv
ev: IEA
syndrome OMIM 602361
Gracile Bone Dysplasia
ev: TAS
syndrome OMIM 306400
Granulomatous Disease, Chronic, X-Linked
freq: 1/1 ev: PCS
syndrome OMIM 232500
Gsd Iv, Classic Hepatic
ev: IEA
syndrome OMIM 232500
Gsd Iv, Neuromuscular Form, Childhood
ev: IEA
syndrome OMIM 232500
Gsd Iv, Neuromuscular Form, Congenital
ev: IEA
syndrome OMIM 232500
Gsd Iv, Neuromuscular Form, Fatal Perinatal
ev: IEA
syndrome OMIM 235200
Hemochromatosis, Type 1
ev: IEA
syndrome OMIM 277900
Hepatolenticular Degeneration
freq: 1/1 ev: PCS
syndrome OMIM 617021
Hydrops, Lactic Acidosis, And Sideroblastic Anemia
freq: 1/1 ev: PCS
syndrome OMIM 615758
Immunodeficiency 22
freq: 1/1 ev: PCS
syndrome OMIM 215600
Indian Childhood Cirrhosis
freq: 1/1 ev: PCS
syndrome OMIM 269920
Infantile Sialic Acid Storage Disease
ev: IEA
syndrome OMIM 243800
Johanson-Blizzard Syndrome
freq: 1/1 ev: PCS
syndrome OMIM 256550
Lipomucopolysaccharidosis
ev: TAS
disease OMIM 265300
Lymphangiectasia, Pulmonary, Congenital
ev: TAS
📜 Formulas studied for Ascites
2 · text-bridged via indications + syndromes