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:
Abnormality of bone marrow cell morphology (HP:0005561)

Parent Node:
Abnormal megakaryocyte morphology (HP:0012143)

..Starting node
..Increased multinucleated megakaryocyte count (HP:0031387)

Term ID:

31387

Name:

Increased multinucleated megakaryocyte count

Synonym:

Definition:

The presence of abnormally high numbers of multinucleated megakaryocytes in the bone marrow.

Comments:

Reference:

HP:0031387

Genes and Diseases:

Child Nodes:

Sister Nodes:

Increased megakaryocyte count (HP:0005513)

Increased micromegakaryocyte count (HP:0031386)

Megakaryocyte dysplasia (HP:0031689)

Megakaryocyte nucleus hyperlobulation (HP:0031388)

Megakaryocyte nucleus hypolobulation (HP:0031385)

Megakaryocytopenia (HP:0005548)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031387	HP:0031387	Increased multinucleated megakaryocyte count	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.