Human Phenotype Ontology 
Grandparent Node:
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Abnormal muscle physiology (HP:0011804)help
Parent Node:
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Muscle stiffness (HP:0003552)help
..Starting node
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Exercise-induced muscle stiffness (HP:0008967)help
Term ID: 8967
Name: Exercise-induced muscle stiffness
Synonym: Exercise-induced muscle stiffness; Muscle stiffness with exercise; Muscle stiffness, exercise-induced
Definition: A type of muscle stiffness that occurs following physical exertion.
Comments:
Reference: HP:0008967
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAsymmetric limb muscle stiffness (HP:0007156) help
..expandAxial muscle stiffness (HP:0006921) help
..expandLeg muscle stiffness (HP:0008969) help
..expandProximal limb muscle stiffness (HP:0007066) 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:0008967HP:0008967Exercise-induced muscle stiffness0ATP2A1 CL E G H487811OMIM:601003BRODY MYOPATHY80
HP:0008967HP:0008967Exercise-induced muscle stiffness0CAV3 CL E G H8591529OMIM:606072Rippling muscle disease.148
HP:0008967HP:0008967Exercise-induced muscle stiffness0MLIP CL E G H9052321355OMIM:620138
HP:0008967HP:0008967Exercise-induced muscle stiffness0PHKA1 CL E G H52558925OMIM:300559Muscle glycogenosis, X-linked.54
HP:0008967HP:0008967Exercise-induced muscle stiffness0PYGM CL E G H58379726ORPHA:368Glycogen storage disease due to muscle glycogen phosphorylase deficiencyHP:0040283 - Occasional166
HP:0008967HP:0008967Exercise-induced muscle stiffness0SCN4A CL E G H632910591ORPHA:99734Myotonia fluctuansHP:0040282 - Frequent263
HP:0008967HP:0008967Exercise-induced muscle stiffness0SLC16A1 CL E G H656610922OMIM:245340Erythrocyte lactate transporter defect.74


Genes (7) :ATP2A1 CAV3 MLIP PHKA1 PYGM SCN4A SLC16A1

Diseases (7) :OMIM:601003 OMIM:606072 OMIM:620138 OMIM:300559 ORPHA:368 ORPHA:99734 OMIM:245340
 

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