Human Phenotype Ontology 
Grandparent Node:
expandAbnormal brainstem morphology (HP:0002363)help
Parent Node:
expandAbnormal brainstem MRI signal intensity (HP:0012747)help
..Starting node
..expandT2 hypointense brainstem (HP:0012750)help
Term ID: 12750
Name: T2 hypointense brainstem
Synonym:
Definition: A darker than expected T2 signal on magnetic resonance imaging (MRI) of the brainstem. This term refers to a diffuse hypointensity affecting the entire brainstem.
Comments:
Reference: HP:0012750
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandFocal T2 hyperintense brainstem lesion (HP:0012748) help
..expandFocal T2 hypointense brainstem lesion (HP:0012749) 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:0012750HP:0012750T2 hypointense brainstem0 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 December 15 2022 release.