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:
Morphological central nervous system abnormality (HP:0002011)

Parent Node:
Abnormal glial cell morphology (HP:0100705)

..Starting node
..Abnormal microglia morphology (HP:0100708)

Term ID:

100708

Name:

Abnormal microglia morphology

Synonym:

Abnormality of the microglia

Definition:

An abnormality of the microglial cells. They are also known as brain-resident macrophages or Hortega cells.

Comments:

Reference:

HP:0100708

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormal astrocyte morphology (HP:0100707)

Abnormal oligodendroglia morphology (HP:0100706)

Astrocytosis (HP:0002446)

Glioma (HP:0009733)

Gliosis (HP:0002171)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100708	HP:0100708	Abnormal microglia morphology	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.