Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of urine homeostasis (HP:0003110)help
Parent Node:
expandMyoglobinuria (HP:0002913)help
..Starting node
..expandRecurrent myoglobinuria (HP:0003652)help
Term ID: 3652
Name: Recurrent myoglobinuria
Synonym: Myoglobinuria, episodic; Myoglobinuria, recurrent
Definition: Recurring episodes of myoglobinuria, i.e., of the presence of myoglobin in the urine. This is usually a consequence of rhabdomyolysis, i.e., of the destruction of muscle tissue.
Comments:
Reference: HP:0003652
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandExercise-induced myoglobinuria (HP:0008305) 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:0003652HP:0003652Recurrent myoglobinuria0COQ2 CL E G H2723525223OMIM:607426Coenzyme Q10 deficiency, primary, 1.54
HP:0003652HP:0003652Recurrent myoglobinuria0COX1 CL E G H45127419ORPHA:99845Genetic recurrent myoglobinuria
HP:0003652HP:0003652Recurrent myoglobinuria0COX3 CL E G H45147422ORPHA:99845Genetic recurrent myoglobinuria
HP:0003652HP:0003652Recurrent myoglobinuria0LPIN1 CL E G H2317513345ORPHA:99845Genetic recurrent myoglobinuria95
HP:0003652HP:0003652Recurrent myoglobinuria0PYGM CL E G H58379726ORPHA:368Glycogen storage disease due to muscle glycogen phosphorylase deficiencyHP:0040282 - Frequent166


Genes (5) :COQ2 COX1 COX3 LPIN1 PYGM

Diseases (3) :OMIM:607426 ORPHA:99845 ORPHA:368
 

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