Human Phenotype Ontology 
Grandparent Node:
expandMorphological central nervous system abnormality (HP:0002011)help
Parent Node:
expandAbnormality of the spinal cord (HP:0002143)help
..Starting node
..expandHyperintensity of MRI T2 signal of the spinal cord (HP:0040272)help
Term ID: 40272
Name: Hyperintensity of MRI T2 signal of the spinal cord
Synonym:
Definition: A region of high intensity (brightness) observed upon magnetic resonance imaging (MRI) scans of the spinal cord.
Comments:
Reference: HP:0040272
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal spinal meningeal morphology (HP:0010303) help
..expandAbnormality of the dorsal column of the spinal cord (HP:0011397) help
..expandAbnormality of the spinocerebellar tracts (HP:0003133) help
..expandAtrophy/Degeneration involving the spinal cord (HP:0007344) help
..expandCervicomedullary schisis (HP:0030325) help
..expandLong-tract signs (HP:0002423) help
..expandMyelitis (HP:0012486) help
..expandMyelopathy (HP:0002196) help
..expandSpinal arteriovenous malformation (HP:0002390) help
..expandSpinal cord compression (HP:0002176) help
..expandSpinal cord lesion (HP:0100561) help
..expandSpinal cord posterior columns myelin loss (HP:0008311) help
..expandSpinal cord tumor (HP:0010302) help
..expandSpinal dysraphism (HP:0010301) help
..expandTethered cord (HP:0002144) 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:0040272HP:0040272Hyperintensity of MRI T2 signal of the spinal cord0FLVCR1 CL E G H2898224682OMIM:609033Ataxia, posterior column, with retinitis pigmentosa111


Genes (1) :FLVCR1

Diseases (1) :OMIM:609033
 

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