Human Phenotype Ontology 
Grandparent Node:
expandMode of inheritance (HP:0000005)help
Parent Node:
expandMultifactorial inheritance (HP:0001426)help
..Starting node
..expandOligogenic inheritance (HP:0010983)help
Term ID: 10983
Name: Oligogenic inheritance
Synonym:
Definition: A type of multifactorial inheritance governed by the simultaneous action of a few gene loci. It is recommended this term be used for traits governed by three loci, although it is noted that usage of this term in the literature is not uniform.
Comments:
Reference: HP:0010983
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandDigenic inheritance (HP:0010984) help
..expandPolygenic inheritance (HP:0010982) 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:0010983HP:0010983Oligogenic inheritance0FLRT3 CL E G H237673762OMIM:615271Hypogonadotropic hypogonadism 21 with or without anosmia4
HP:0010983HP:0010983Oligogenic inheritance0GJA1 CL E G H26974274OMIM:241550HYPOPLASTIC LEFT HEART SYNDROME 1; HLHS168


Genes (2) :FLRT3 GJA1

Diseases (2) :OMIM:615271 OMIM:241550
 

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