Human Phenotype Ontology 
Grandparent Node:
expandAbnormal cerebral subcortex morphology (HP:0010993)help
Parent Node:
expandAbnormal cerebral white matter morphology (HP:0002500)help
..Starting node
..expandAbnormality of the bed nucleus of stria terminalis (HP:0030798)help
Term ID: 30798
Name: Abnormality of the bed nucleus of stria terminalis
Synonym:
Definition: The stria terminalis is a slender, compact fiber bundle that connects the amygdala (amygdaloid body) with the hypothalamus and other basal forebrain regions. The bed nucleus of the stria terminalis is a limbic forebrain structure that receives heavy projections from, among other areas, the basolateral amygdala, and projects in turn to hypothalamic and brainstem target areas that mediate many of the autonomic and behavioral responses to aversive or threatening stimuli. This term refers to an anomaly of the bed nucleus.
Comments:
Reference: HP:0030798
Genes and Diseases:
 
       Child Nodes:
........expandReduced volume of central subdivision of bed nucleus of stria terminalis (HP:0030797) help

 Sister Nodes: 
..expandAbnormal corpus callosum morphology (HP:0001273) help
..expandAbnormal periventricular white matter morphology (HP:0002518) help
..expandAbnormality of the anterior commissure (HP:0030301) help
..expandAbnormality of the internal capsule (HP:0012502) help
..expandAplasia/Hypoplasia of the cerebral white matter (HP:0012429) help
..expandCerebral white matter atrophy (HP:0012762) help
..expandDiffuse swelling of cerebral white matter (HP:0007341) help
..expandDiffuse white matter abnormalities (HP:0007204) help
..expandFocal white matter lesions (HP:0007042) help
..expandHyperintensity of cerebral white matter on MRI (HP:0030890) help
..expandHypointensity of cerebral white matter on MRI (HP:0007103) help
..expandMultifocal cerebral white matter abnormalities (HP:0007052) help
..expandSubcortical white matter calcifications (HP:0007346) help
..expandWhite mater abnormalities in the posterior periventricular region (HP:0006812) 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:0030798HP:0030798Abnormality of the bed nucleus of stria terminalis0 CL E G H
HP:0030798HP:0030797Reduced volume of central subdivision of bed nucleus of stria terminalis1 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.