Human Phenotype Ontology 
Grandparent Node:
expandCentral nervous system cyst (HP:0030724)help
Parent Node:
expandIntracranial cystic lesion (HP:0010576)help
..Starting node
..expandIntracranial epidermoid cyst (HP:0012096)help
Term ID: 12096
Name: Intracranial epidermoid cyst
Synonym:
Definition: A congenital inclusion cysts that arises from ectodermal cells that normally form skin cells being left behind in the nervous system during development.
Comments:
Reference: HP:0012096
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBasal ganglia cysts (HP:0006799) help
..expandCerebellar cyst (HP:0002350) help
..expandIntracranial dermoid cyst (HP:0012097) help
..expandPeriventricular cysts (HP:0007109) help
..expandPosterior fossa cyst (HP:0007291) help
..expandSubependymal cysts (HP:0002416) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012096HP:0012096Intracranial epidermoid cyst0 CL E G H


Genes (0) :

Diseases (0) :
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.