Human Phenotype Ontology 
Grandparent Node:
Abnormal choroid morphology (HP:0000610)help
Grandparent Node:
Abnormal retinal morphology (HP:0000479)help
Parent Node:
Abnormal chorioretinal morphology (HP:0000532)help
..Starting node
Central serous chorioretinopathy (HP:0025567)help
Term ID: 25567
Name: Central serous chorioretinopathy
Definition: An anomaly of the retina with serous detachment of the neurosensory retina secondary to one or more focal lesions of the retinal pigment epithelium (RPE), and associated with blurred vision, usually in one eye only and perceived typically by the patient as a dark spot in the centre of the visual field with associated micropsia and metamorphopsia. Normal vision often recurs spontaneously within a few months.
Reference: HP:0025567
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandAbnormality of chorioretinal pigmentation (HP:0007661) help
..expandChorioretinal coloboma (HP:0000567) help
..expandChorioretinal degeneration (HP:0200065) help
..expandChorioretinal dysplasia (HP:0007731) help
..expandChorioretinal dystrophy (HP:0001135) help
..expandChorioretinal lacunae (HP:0007858) help
..expandChorioretinitis (HP:0012424) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025567HP:0025567Central serous chorioretinopathy0 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 August 2021 release.