Human Phenotype Ontology 
Grandparent Node:
expand
Abnormal foveal morphology on macular OCT (HP:0030613)help
Parent Node:
expand
Abnormal OCT-measured foveal thickness (HP:0030617)help
..Starting node
..expand
Reduced OCT-measured foveal thickness (HP:0030619)help
Term ID: 30619
Name: Reduced OCT-measured foveal thickness
Synonym:
Definition:
Comments:
Reference: HP:0030619
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandIncreased OCT-measured foveal thickness (HP:0030618) 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:0030619HP:0030619Reduced OCT-measured foveal thickness0CLEC3B CL E G H712311891OMIM:619977


Genes (1) :CLEC3B

Diseases (1) :OMIM:619977
 

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