Human Phenotype Ontology 
Grandparent Node:
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Abnormality of fluid regulation (HP:0011032)help
Parent Node:
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Abnormal lung morphology (HP:0002088)help
Parent Node:
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Edema (HP:0000969)help
..Starting node
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Pulmonary edema (HP:0100598)help
Term ID: 100598
Name: Pulmonary edema
Synonym: Excess fluid in lungs; Lung edema; Lung oedema; Pulmonary oedema; Wet lung
Definition: Fluid accumulation in the lungs.
Comments:
Reference: HP:0100598
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
..expandHypoproteinemic edema (HP:0007609) 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
..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:0100598HP:0100598Pulmonary edema0ABCA3 CL E G H2133ORPHA:70587Infant acute respiratory distress syndromeHP:0040282 - Frequent147
HP:0100598HP:0100598Pulmonary edema0CD46 CL E G H41796953ORPHA:244242HELLP syndromeHP:0040283 - Occasional39
HP:0100598HP:0100598Pulmonary edema0CFH CL E G H30754883ORPHA:244242HELLP syndromeHP:0040283 - Occasional86
HP:0100598HP:0100598Pulmonary edema0CFI CL E G H34265394ORPHA:244242HELLP syndromeHP:0040283 - Occasional57
HP:0100598HP:0100598Pulmonary edema0CYTB CL E G H45197427ORPHA:137675Histiocytoid cardiomyopathyHP:0040284 - Very rare
HP:0100598HP:0100598Pulmonary edema0EIF2AK4 CL E G H44027519687ORPHA:199241Pulmonary capillary hemangiomatosisHP:0040283 - Occasional40
HP:0100598HP:0100598Pulmonary edema0EPHB4 CL E G H20503395OMIM:617300Lymphatic malformation 7.3
HP:0100598HP:0100598Pulmonary edema0FLNC CL E G H23183756ORPHA:75249Familial isolated restrictive cardiomyopathyHP:0040283 - Occasional197
HP:0100598HP:0100598Pulmonary edema0FOCAD CL E G H5491423377OMIM:6199913
HP:0100598HP:0100598Pulmonary edema0FSHR CL E G H24923969ORPHA:64739Ovarian hyperstimulation syndromeHP:0040283 - Occasional50
HP:0100598HP:0100598Pulmonary edema0HELLPAR CL E G H10110169243984ORPHA:244242HELLP syndromeHP:0040283 - Occasional
HP:0100598HP:0100598Pulmonary edema0KIF20A CL E G H101129787ORPHA:75249Familial isolated restrictive cardiomyopathyHP:0040283 - Occasional
HP:0100598HP:0100598Pulmonary edema0MOGS CL E G H784124862ORPHA:79330MOGS-CDGHP:0040283 - Occasional37
HP:0100598HP:0100598Pulmonary edema0MYBPC3 CL E G H46077551OMIM:115197Cardiomyopathy, familial hypertrophic, 4.1143
HP:0100598HP:0100598Pulmonary edema0MYPN CL E G H8466523246ORPHA:75249Familial isolated restrictive cardiomyopathyHP:0040283 - Occasional217
HP:0100598HP:0100598Pulmonary edema0NAA10 CL E G H826018704OMIM:300855Ogden syndrome23
HP:0100598HP:0100598Pulmonary edema0NKX2-6 CL E G H13781432940ORPHA:3384Truncus arteriosusHP:0040283 - Occasional3
HP:0100598HP:0100598Pulmonary edema0PLXND1 CL E G H231299107ORPHA:3384Truncus arteriosusHP:0040283 - Occasional
HP:0100598HP:0100598Pulmonary edema0PRKAG2 CL E G H514229386OMIM:261740Glycogen storage disease of heart, lethal congenital.235
HP:0100598HP:0100598Pulmonary edema0SFTPB CL E G H643910801ORPHA:70587Infant acute respiratory distress syndromeHP:0040282 - Frequent51
HP:0100598HP:0100598Pulmonary edema0SFTPC CL E G H644010802ORPHA:70587Infant acute respiratory distress syndromeHP:0040282 - Frequent33
HP:0100598HP:0100598Pulmonary edema0TNNI3 CL E G H713711947ORPHA:75249Familial isolated restrictive cardiomyopathyHP:0040283 - Occasional180
HP:0100598HP:0100598Pulmonary edema0TNNT2 CL E G H713911949ORPHA:75249Familial isolated restrictive cardiomyopathyHP:0040283 - Occasional248


Genes (23) :ABCA3 CD46 CFH CFI CYTB EIF2AK4 EPHB4 FLNC FOCAD FSHR HELLPAR KIF20A MOGS MYBPC3 MYPN NAA10 NKX2-6 PLXND1 PRKAG2 SFTPB SFTPC TNNI3 TNNT2

Diseases (13) :ORPHA:70587 ORPHA:244242 ORPHA:137675 ORPHA:199241 OMIM:617300 ORPHA:75249 OMIM:619991 ORPHA:64739 ORPHA:79330 OMIM:115197 OMIM:300855 ORPHA:3384 OMIM:261740
 

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