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 leukocyte morphology (HP:0001881)

Parent Node:
Abnormal lymphocyte morphology (HP:0004332)

..Starting node
..Plasmacytosis (HP:0030150)

Term ID:

30150

Name:

Plasmacytosis

Synonym:

Definition:

An abnormally increased number of plasma cells in tissues, exudates, or blood

Comments:

Reference:

HP:0030150

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormal B cell morphology (HP:0002846)

Abnormal lymphocyte count (HP:0040088)

Abnormal natural killer cell morphology (HP:0012176)

Abnormal T cell morphology (HP:0002843)

Absent microvilli on the surface of peripheral blood lymphocytes (HP:0002971)

Impaired lymphocyte transformation with phytohemagglutinin (HP:0003347)

Lymphocytosis (HP:0100827)

Lymphopenia (HP:0001888)

Vacuolated lymphocytes (HP:0001922)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030150	HP:0030150	Plasmacytosis	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.