Human Phenotype Ontology 
Grandparent Node:
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Abnormal abdomen morphology (HP:0001438)help
Parent Node:
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Abnormality of prenatal development or birth (HP:0001197)help
Parent Node:
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Ascites (HP:0001541)help
..Starting node
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Fetal ascites (HP:0001791)help
Term ID: 1791
Name: Fetal ascites
Synonym: Foetal ascites
Definition: Accumulation of fluid in the peritoneal cavity during the fetal period.
Comments:
Reference: HP:0001791
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandChylous ascites (HP:0012281) help
..expandEosinophilic ascites (HP:0031780) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0001791HP:0001791Fetal ascites0EIF5A CL E G H19843300OMIM:619376FAUNDES-BANKA SYNDROME; FABAS
HP:0001791HP:0001791Fetal ascites0GNB2 CL E G H27834398OMIM:619503NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND DYSMORPHIC FACIES; NEDHYDF
HP:0001791HP:0001791Fetal ascites0HSD17B4 CL E G H32955213OMIM:261515D-bifunctional protein deficiency.98
HP:0001791HP:0001791Fetal ascites0MDFIC CL E G H2996928870OMIM:620014
HP:0001791HP:0001791Fetal ascites0NPC1 CL E G H48647897OMIM:257220Niemann-pick disease, type C1.258
HP:0001791HP:0001791Fetal ascites0NPC2 CL E G H1057714537OMIM:607625Niemann-pick disease, type C2.33
HP:0001791HP:0001791Fetal ascites0RHD CL E G H600710009OMIM:619462Hemolytic disease of fetus and newborn, RH-induced16


Genes (7) :EIF5A GNB2 HSD17B4 MDFIC NPC1 NPC2 RHD

Diseases (7) :OMIM:619376 OMIM:619503 OMIM:261515 OMIM:620014 OMIM:257220 OMIM:607625 OMIM:619462
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.