Human Phenotype Ontology 
Grandparent Node:
expandAbnormal cerebral morphology (HP:0002060)help
Parent Node:
expandAbnormal septum pellucidum morphology (HP:0007375)help
..Starting node
..expandPartial absence of the septum pellucidum (HP:0030283)help
Term ID: 30283
Name: Partial absence of the septum pellucidum
Synonym:
Definition: Only part of the septum pellucidum (a thin, triangular, vertical membrane separating the lateral ventricles of the brain) is present. This feature can be appreciated on magnetic resonance tomography or computed tomography of the brain.
Comments:
Reference: HP:0030283
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbsent septum pellucidum (HP:0001331) help
..expandCavum septum pellucidum (HP:0002389) 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:0030283HP:0030283Partial absence of the septum pellucidum0 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.