Human Phenotype Ontology 
Grandparent Node:
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Abnormality of urine homeostasis (HP:0003110)help
Parent Node:
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Myoglobinuria (HP:0002913)help
..Starting node
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Exercise-induced myoglobinuria (HP:0008305)help
Term ID: 8305
Name: Exercise-induced myoglobinuria
Synonym: Exercise-induced myoglobinuria in adults
Definition: Presence of myoglobin in the urine following exercise.
Comments:
Reference: HP:0008305
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandRecurrent myoglobinuria (HP:0003652) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0008305HP:0008305Exercise-induced myoglobinuria0ACADL CL E G H3399900ORPHA13588609576
HP:0008305HP:0008305Exercise-induced myoglobinuria0ACADL CL E G H3399900ORPHA13388609576
HP:0008305HP:0008305Exercise-induced myoglobinuria0ACADVL CL E G H37201475Very long chain acyl-CoA dehydrogenase deficiency201475C3887523OMIM1111692609575
HP:0008305HP:0008305Exercise-induced myoglobinuria0ACADVL CL E G H37201475Very long chain acyl-CoA dehydrogenase deficiency201475C3887523OMIM197892609575
HP:0008305HP:0008305Exercise-induced myoglobinuria0PFKM CL E G H5213232800Glycogen storage disease, type VII232800C0017926OMIM13778877610681
HP:0008305HP:0008305Exercise-induced myoglobinuria0PFKM CL E G H5213232800Glycogen storage disease, type VII232800C0017926OMIM13438877610681
HP:0008305HP:0008305Exercise-induced myoglobinuria0PGK1 CL E G H5230300653Phosphoglycerate kinase 1 deficiency300653C1970848OMIM12458896311800
HP:0008305HP:0008305Exercise-induced myoglobinuria0PGK1 CL E G H5230300653Phosphoglycerate kinase 1 deficiency300653C1970848OMIM12288896311800
HP:0008305HP:0008305Exercise-induced myoglobinuria0PHKA1 CL E G H5255300559Glycogen storage disease IXd300559C1845151OMIM13848925311870
HP:0008305HP:0008305Exercise-induced myoglobinuria0PHKA1 CL E G H5255300559Glycogen storage disease IXd300559C1845151OMIM13558925311870
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0008305HP:0008305Exercise-induced myoglobinuria0FKRP CL E G H79147607155Limb-girdle muscular dystrophy-dystroglycanopathy, type C5607155C1846672OMIM067117997606596
HP:0008305HP:0008305Exercise-induced myoglobinuria0FKRP CL E G H79147607155Limb-girdle muscular dystrophy-dystroglycanopathy, type C5607155C1846672OMIM057217997606596
HP:0008305HP:0008305Exercise-induced myoglobinuria0ISPD CL E G H729920352479ORPHA054937276614631
HP:0008305HP:0008305Exercise-induced myoglobinuria0ISPD CL E G H729920352479ORPHA054537276614631


Genes (7) :ACADL ACADVL CRPPA FKRP PFKM PGK1 PHKA1

Diseases (7) :99900 201475 352479 607155 232800 300653 300559
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.