Human Phenotype Ontology 
Grandparent Node:
expandGeneralized non-motor (absence) seizure (HP:0002121)help
Parent Node:
expandobsolete Absence seizures with special features (HP:0011148)help
..Starting node
..expandAbsence seizure with eyelid myoclonia (HP:0011149)help
Term ID: 11149
Name: Absence seizure with eyelid myoclonia
Synonym: Absence seizures with eyelid myoclonia
Definition: An absence with eyelid myoclonia seizure is a type of generalized non-motor (absence) seizure characterised by forced upward jerking of the eyelids during an absence seizure.
Comments:
Reference: HP:0011149
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandMyoclonic absence seizure (HP:0011150) 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:0011149HP:0011149Absence seizure with eyelid myoclonia0AP2M1 CL E G H1173564OMIM:618587INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 60, WITH SEIZURES; MRD60


Genes (1) :AP2M1

Diseases (1) :OMIM:618587
 

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