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 vitreous humor morphology (HP:0004327)

Parent Node:
Vitritis (HP:0011531)

..Starting node
..Vitreous inflammatory cells (HP:0030662)

Term ID:

30662

Name:

Vitreous inflammatory cells

Synonym:

Definition:

The presence of inflammatory cells such as lymphocytes and macrophages in the vitreous.

Comments:

Reference:

HP:0030662

Genes and Diseases:

Child Nodes:

Sister Nodes:

Vitreous haze (HP:0030652)

Vitreous snowballs (HP:0030661)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030662	HP:0030662	Vitreous inflammatory cells	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.