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:
Yellow/white lesions of the retina (HP:0030506)

Parent Node:
Retinal exudate (HP:0001147)

..Starting node
..Subretinal exudate (HP:0011532)

Term ID:

11532

Name:

Subretinal exudate

Synonym:

Definition:

A type of retinal exudate located in the subretinal space between the sensory retina and the retinal pigment epithelium.

Comments:

Reference:

HP:0011532

Genes and Diseases:

Child Nodes:

Sister Nodes:

Central retinal exudate (HP:0007822)

Exudative retinopathy (HP:0007898)

Intraretinal exudate (HP:0007989)

Peripapillary exudate (HP:0025093)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011532	HP:0011532	Subretinal exudate	0	NDP CL E G H	4693	7678	OMIM:305390	Exudative vitreoretinopathy 2, X-linked	39

Genes (1) :NDP

Diseases (1) :OMIM:305390

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.