Human Phenotype Ontology 
Grandparent Node:
expandCentral nervous system cyst (HP:0030724)help
Parent Node:
expandIntracranial cystic lesion (HP:0010576)help
..Starting node
..expandIntracranial dermoid cyst (HP:0012097)help
Term ID: 12097
Name: Intracranial dermoid cyst
Synonym:
Definition: A congenital inclusion cysts that arises from the inclusion of ectodermally committed cells at the time of neural tube closure (3rd-5th week of embryogenesis). The capsule of dermoid cysts consists of simple epithelium supported by collagen. In thicker parts, the lining is supplemented with dermis containing hair follicles, sebaceous glands, and apocrine glands.
Comments:
Reference: HP:0012097
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBasal ganglia cysts (HP:0006799) help
..expandCerebellar cyst (HP:0002350) help
..expandIntracranial epidermoid cyst (HP:0012096) 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:0012097HP:0012097Intracranial dermoid 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.