Human Phenotype Ontology 
Grandparent Node:
expandMorphological central nervous system abnormality (HP:0002011)help
Parent Node:
expandAbnormality of olfactory lobe morphology (HP:0025057)help
Parent Node:
expandAplasia/Hypoplasia involving the central nervous system (HP:0002977)help
..Starting node
..expandHypoplastic olfactory lobes (HP:0006894)help
Term ID: 6894
Name: Hypoplastic olfactory lobes
Synonym:
Definition:
Comments:
Reference: HP:0006894
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAgenesis of pineal gland (HP:0012687) help
..expandAplasia/Hypoplasia involving the corticospinal tracts (HP:0007365) help
..expandAplasia/Hypoplasia of the brainstem (HP:0007362) help
..expandAplasia/Hypoplasia of the cerebellum (HP:0007360) help
..expandAplasia/Hypoplasia of the cerebrum (HP:0007364) help
..expandAplasia/Hypoplasia of the optic tract (HP:0011000) help
..expandAplasia/Hypoplasia of the pyramidal tract (HP:0007363) help
..expandAtrophy/Degeneration affecting the cerebrum (HP:0007369) help
..expandGlobal brain atrophy (HP:0002283) help
..expandHypoplasia of olfactory tract (HP:0007036) help
..expandHypoplasia of the olfactory bulb (HP:0040326) help
..expandOptic nerve hypoplasia (HP:0000609) 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:0006894HP:0006894Hypoplastic olfactory lobes0PEX1 CL E G H51898850OMIM:214100Peroxisome biogenesis disorder 1A (Zellweger).169


Genes (1) :PEX1

Diseases (1) :OMIM:214100
 

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