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 myeloid cell morphology (HP:0020047)

Parent Node:
Abnormal erythroid lineage cell morphology (HP:0012130)

..Starting node
..Abnormal morphology of erythroid progenitor cell (HP:0025034)

Term ID:

25034

Name:

Abnormal morphology of erythroid progenitor cell

Synonym:

Definition:

Abnormal form of the progenitor cells committed to the erythroid lineage.

Comments:

Reference:

HP:0025034

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormal proerythroblast morphology (HP:0025035)

Erythroid dysplasia (HP:0031688)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025034	HP:0025034	Abnormal morphology of erythroid progenitor cell	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.