Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

..Starting node
..Monoclonal elevation of IgG light chain (HP:0032292)

Term ID:

32292

Name:

Monoclonal elevation of IgG light chain

Synonym:

Definition:

A type of monoclonal elevation of IgG in which the involved immunoglobulin has an abnormal structure with a light chain but not a heavy chain.

Comments:

Reference:

HP:0032292

Genes and Diseases:

Child Nodes:

Sister Nodes:

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0032292	HP:0032292	Monoclonal elevation of IgG light chain	0	CL E G H
HP:0032292	HP:0032295	Monoclonal elevation of IgG lambda chain	1	CL E G H
HP:0032292	HP:0032294	Monoclonal elevation of IgG kappa chain	1	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.