Human Phenotype Ontology

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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
..Decreased circulating IgG3 level (HP:0032137)

Term ID:

32137

Name:

Decreased circulating IgG3 level

Synonym:

Decreased IgG3 level in blood

Definition:

A reduction in immunoglobulin levels of the IgG3 subclass in the blood circulation.

Comments:

Reference:

HP:0032137

Genes and Diseases:

Child Nodes:

Sister Nodes:

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0032137	HP:0032137	Decreased circulating IgG3 level	0	IFIH1 CL E G H	64135	18873	OMIM:619773	IMMUNODEFICIENCY 95; IMD95	28
HP:0032137	HP:0041072	Chronic decreased circulating IgG3	1	CL E G H
HP:0032137	HP:0041071	Transient decreased circulating IgG3	1	CL E G H
HP:0032137	HP:0041075	Chronic partially decreased circulating IgG3	2	CL E G H
HP:0032137	HP:0041074	Chronic (near) absent circulating IgG3	2	CL E G H

Genes (1) :IFIH1

Diseases (1) :OMIM:619773

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