Human Phenotype Ontology 
Grandparent Node:
Abnormality of movement (HP:0100022)help
Parent Node:
Involuntary movements (HP:0004305)help
..Starting node
Intermittent painful muscle spasms (HP:0011964)help
Term ID: 11964
Name: Intermittent painful muscle spasms
Definition: History of repeated intermittent involuntary muscle contractions that were painful.
Reference: HP:0011964
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandAthetosis (HP:0002305) help
..expandChorea (HP:0002072) help
..expandClonus (HP:0002169) help
..expandFasciculations (HP:0002380) help
..expandHemiballismus (HP:0100248) help
..expandMotor stereotypy (HP:0000733) help
..expandMyoclonus (HP:0001336) help
..expandParoxysmal dyskinesia (HP:0007166) help
..expandSelf-mutilation of tongue and lips due to involuntary movements (HP:0008767) help
..expandTics (HP:0100033) help
..expandTremor (HP:0001337) 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:0011964HP:0011964Intermittent painful muscle spasms0CACNA1S CL E G H7791397ORPHA:423Malignant hyperthermia of anesthesiaHP:0040282 - Frequent247
HP:0011964HP:0011964Intermittent painful muscle spasms0CPT2 CL E G H13762330ORPHA:228302Carnitine palmitoyl transferase II deficiency, myopathic formHP:0040283 - Occasional101
HP:0011964HP:0011964Intermittent painful muscle spasms0CPT2 CL E G H13762330ORPHA:228305Carnitine palmitoyl transferase II deficiency, severe infantile formHP:0040282 - Frequent101
HP:0011964HP:0011964Intermittent painful muscle spasms0RYR1 CL E G H626110483ORPHA:423Malignant hyperthermia of anesthesiaHP:0040282 - Frequent1200
HP:0011964HP:0011964Intermittent painful muscle spasms0TFG CL E G H1034211758ORPHA:90117Hereditary motor and sensory neuropathy, Okinawa typeHP:0040281 - Very frequent18

Genes (4) :CACNA1S CPT2 RYR1 TFG

Diseases (4) :ORPHA:423 ORPHA:228302 ORPHA:228305 ORPHA:90117

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