Human Phenotype Ontology 
Grandparent Node:
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Asymmetry of iris pigmentation (HP:0200064)help
Parent Node:
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Heterochromia iridis (HP:0001100)help
..Starting node
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Lester's sign (HP:0009781)help
Term ID: 9781
Name: Lester's sign
Synonym:
Definition: A zone of darker pigmentation around the central part of the iris with a roughly cloverleaf or flower shape.
Comments:
Reference: HP:0009781
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCentral heterochromia (HP:0007818) 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:0009781HP:0009781Lester's sign0LMX1B CL E G H40106654OMIM:161200Nail-Patella syndrome.165
HP:0009781HP:0009781Lester's sign0LMX1B CL E G H40106654ORPHA:2614Nail-patella syndromeHP:0040283 - Occasional165


Genes (1) :LMX1B

Diseases (2) :OMIM:161200 ORPHA:2614
 

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