Human Phenotype Ontology 
Grandparent Node:
expandAbnormal arachnoid mater morphology (HP:0100700)help
Parent Node:
expandArachnoid cyst (HP:0100702)help
..Starting node
..expandSuprasellar arachnoid cyst (HP:0012489)help
Term ID: 12489
Name: Suprasellar arachnoid cyst
Synonym:
Definition: An arachnoid cyst that progressively enlarges from an abnormality in the membrane of Liliequist or in the interpeduncular cistern, and typically, expands from the prepontine space, displacing the floor of the third ventricle upwards, the pituitary stalk and optic chiasm upwards and forwards, and the mammillary bodies upwards and backwards.
Comments:
Reference: HP:0012489
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCerebellopontine angle arachnoid cyst (HP:0012487) help
..expandIntraventricular arachnoid cyst (HP:0012488) help
..expandSpinal arachnoid cyst (HP:0009745) 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:0012489HP:0012489Suprasellar arachnoid cyst0TMEM231 CL E G H7958337234ORPHA:2752Orofaciodigital syndrome type 3HP:0040282 - Frequent33


Genes (1) :TMEM231

Diseases (1) :ORPHA:2752
 

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