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

Grandparent Node:
Abnormal cellular physiology (HP:0011017)

Grandparent Node:
Abnormal lymphocyte physiology (HP:0031409)

Parent Node:
Abnormality of T cell physiology (HP:0011840)

..Starting node
..obsolete Exaggerated cellular immune processes (HP:0005397)

Term ID:

5397

Name:

obsolete Exaggerated cellular immune processes

Synonym:

Definition:

Comments:

Reference:

HP:0005397

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormal delayed hypersensitivity skin test (HP:0002963)

Abnormal T cell activation (HP:0410035)

Abnormal T cell proliferation (HP:0031379)

Impaired T cell function (HP:0005435)

Lack of T cell function (HP:0005354)

Oligoclonal T cell expansion (HP:0031430)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0005397	HP:0005397	obsolete Exaggerated cellular immune processes	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.