Human Phenotype Ontology 
Grandparent Node:
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Abnormal optical coherence tomography (HP:0030603)help
Parent Node:
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Abnormal retinal morphology on macular OCT (HP:0030612)help
..Starting node
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Retinal pigment epithelial loss on macular OCT (HP:0030611)help
Term ID: 30611
Name: Retinal pigment epithelial loss on macular OCT
Synonym:
Definition:
Comments:
Reference: HP:0030611
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal foveal morphology on macular OCT (HP:0030613) help
..expandAbnormal OCT-measured macular thickness (HP:0030606) help
..expandHyporeflective spaces on macular OCT (HP:0030625) help
..expandInner retinal layer loss on macular OCT (HP:0030620) help
..expandPhotoreceptor layer loss on macular OCT (HP:0030609) help
..expandPhotoreceptor outer segment loss on macular OCT (HP:0030610) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030611HP:0030611Retinal pigment epithelial loss on macular OCT0 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.