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 fundus morphology (HP:0001098)

Parent Node:
Fundus hemorrhage (HP:0031803)

..Starting node
..Preretinal hemorrhage (HP:0025240)

Term ID:

25240

Name:

Preretinal hemorrhage

Synonym:

Preretinal haemorrhage; Preretinal heme

Definition:

An accumulation of blood between the neurosensory retina and the retinal pigment epithelium (RPE) arising from the choroidal or retinal circulation.

Comments:

Reference:

HP:0025240

Genes and Diseases:

Child Nodes:

........

Subhyaloid hemorrhage (HP:0025239)

........

Premacular hemorrhage (HP:0031804)

Sister Nodes:

Retinal hemorrhage (HP:0000573)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025240	HP:0025240	Preretinal hemorrhage	0	CL E G H
HP:0025240	HP:0025239	Subhyaloid hemorrhage	1	CL E G H
HP:0025240	HP:0031804	Premacular hemorrhage	1	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.