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:
Non-Hodgkin lymphoma (HP:0012539)

Parent Node:
T-cell lymphoma (HP:0012190)

..Starting node
..T-cell lymphoma/leukemia (HP:0005517)

Term ID:

5517

Name:

T-cell lymphoma/leukemia

Synonym:

Definition:

A type of T-cell lymphoma in which cancerous T-cells may present in the blood (leukemia), lymph nodes (lymphoma), skin or in multiple areas.

Comments:

Reference:

HP:0005517

Genes and Diseases:

Child Nodes:

Sister Nodes:

Anaplastic large-cell lymphoma (HP:0012193)

Cutaneous T-cell lymphoma (HP:0012192)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0005517	HP:0005517	T-cell lymphoma/leukemia	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.