Human Phenotype Ontology 
Grandparent Node:
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Abnormality of fluid regulation (HP:0011032)help
Parent Node:
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Edema (HP:0000969)help
..Starting node
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Hypoproteinemic edema (HP:0007609)help
Term ID: 7609
Name: Hypoproteinemic edema
Synonym: Hypoproteinemic oedema
Definition: An abnormal accumulation of fluid beneath the skin, or in one or more cavities of the body because of decreased osmotic pressure of plasma (hypoproteinemia).
Comments:
Reference: HP:0007609
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAngioedema (HP:0100665) help
..expandCerebral edema (HP:0002181) help
..expandCorneal stromal edema (HP:0012040) help
..expandEdema of the dorsum of feet (HP:0012098) help
..expandEdema of the dorsum of hands (HP:0007514) help
..expandEdema of the upper limbs (HP:0010742) help
..expandFacial edema (HP:0000282) help
..expandGeneralized edema (HP:0007430) help
..expandGenital edema (HP:0031188) help
..expandHydrops fetalis (HP:0001789) help
..expandHyperkeratosis over edematous areas (HP:0007448) help
..expandIncreased nuchal translucency (HP:0010880) help
..expandIntestinal edema (HP:0005225) help
..expandJoint swelling (HP:0001386) help
..expandLaryngeal edema (HP:0012027) help
..expandLymphedema (HP:0001004) help
..expandMacular edema (HP:0040049) help
..expandMuscular edema (HP:0100748) help
..expandPeau d'orange (HP:0025533) help
..expandPedal edema (HP:0010741) help
..expandPeripheral edema (HP:0012398) help
..expandPharyngeal edema (HP:0011855) help
..expandPleural effusion (HP:0002202) help
..expandPulmonary edema (HP:0100598) help
..expandTongue edema (HP:0040315) 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:0007609HP:0007609Hypoproteinemic edema0TMPRSS15 CL E G H56519490OMIM:226200Enterokinase deficiency.5


Genes (1) :TMPRSS15

Diseases (1) :OMIM:226200
 

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