Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the musculature (HP:0003011)help
Parent Node:
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Abnormal muscle physiology (HP:0011804)help
..Starting node
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Muscle hyperirritability (HP:0003559)help
Term ID: 3559
Name: Muscle hyperirritability
Synonym:
Definition:
Comments:
Reference: HP:0003559
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal muscle tone (HP:0003808) help
..expandEMG abnormality (HP:0003457) help
..expandFunctional motor deficit (HP:0004302) help
..expandIncreased muscle fatiguability (HP:0003750) help
..expandMuscle spasm (HP:0003394) help
..expandMuscle stiffness (HP:0003552) help
..expandMuscle weakness (HP:0001324) help
..expandMyotonia (HP:0002486) help
..expandTetany (HP:0001281) 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:0003559HP:0003559Muscle hyperirritability0CAV3 CL E G H8591529OMIM:606072Rippling muscle disease.148


Genes (1) :CAV3

Diseases (1) :OMIM:606072
 

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