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

Grandparent Node:
Abnormal CD4-positive, CD25-positive, alpha-beta regulatory T cell morphology (HP:0030334)

Parent Node:
Abnormal CD4-positive, CD25-positive, alpha-beta regulatory T cell count (HP:0030335)

..Starting node
..Absence of CD4-positive, CD25-positive regulatory T cells (HP:0030336)

Term ID:

30336

Name:

Absence of CD4-positive, CD25-positive regulatory T cells

Synonym:

Absence of CD4+CD25+ T regulatory cells; Absence of CD4+CD25+ Tregs

Definition:

Lack of CD4+CD25+ T regulatory cells.

Comments:

Reference:

HP:0030336

Genes and Diseases:

Child Nodes:

Sister Nodes:

Elevated CD4-positive, CD25-positive regulatory T cell count (HP:0030337)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030336	HP:0030336	Absence of CD4-positive, CD25-positive regulatory T cells	0	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.