Human Phenotype Ontology 
Grandparent Node:
expandMultiple central nervous system lipomas (HP:0100251)help
Parent Node:
expandAbnormal corpus callosum morphology (HP:0001273)help
Parent Node:
expandMidline central nervous system lipomas (HP:0006866)help
..Starting node
..expandPericallosal lipoma (HP:0006931)help
Term ID: 6931
Name: Pericallosal lipoma
Synonym: Lipoma of corpus callosum
Definition: Pericallosal lipomas are congenital soft masses of adipose cells encapsulated by a thin layer of fibrous tissue, appearing adjacent to the corpus callosum of the brain.
Comments:
Reference: HP:0006931
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0006931HP:0006931Pericallosal lipoma0ALX1 CL E G H80921494ORPHA:306542Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndromeHP:0040283 - Occasional5
HP:0006931HP:0006931Pericallosal lipoma0ALX3 CL E G H257449OMIM:136760Frontonasal dysplasia 19
HP:0006931HP:0006931Pericallosal lipoma0ALX3 CL E G H257449ORPHA:391474FrontorhinyHP:0040282 - Frequent9
HP:0006931HP:0034014Tubulonodular pericallosal lipoma1 CL E G H
HP:0006931HP:0034013Curvilinear pericallosal lipoma1 CL E G H


Genes (2) :ALX1 ALX3

Diseases (3) :ORPHA:306542 OMIM:136760 ORPHA:391474
 

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