Human Phenotype Ontology 
Grandparent Node:
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Abnormal ocular adnexa morphology (HP:0030669)help
Parent Node:
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Abnormal conjunctiva morphology (HP:0000502)help
..Starting node
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Bitot spots of the conjunctiva (HP:0007462)help
Term ID: 7462
Name: Bitot spots of the conjunctiva
Synonym: Bitot's spots
Definition: Keratinization of the bulbar conjunctiva near the limbus (corneoscleral junction), resulting in a raised spot.
Comments:
Reference: HP:0007462
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal morphology of the conjunctival vasculature (HP:0008054) help
..expandChemosis (HP:0012375) help
..expandConjunctival amyloidosis (HP:0010637) help
..expandConjunctival dermolipoma (HP:0500070) help
..expandConjunctival follicles (HP:0030947) help
..expandConjunctival hamartoma (HP:0100780) help
..expandConjunctival hyperemia (HP:0030953) help
..expandConjunctival lipoma (HP:0012549) help
..expandConjunctival nodule (HP:0009903) help
..expandConjunctival papillae (HP:0030946) help
..expandConjunctival whitish salt-like deposits (HP:0007799) help
..expandConjunctivitis (HP:0000509) help
..expandDefect of palpebral conjunctiva (HP:0430011) help
..expandLimbal dermoid (HP:0001140) help
..expandPinguecula (HP:0031830) 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:0007462HP:0007462Bitot spots of the conjunctiva0 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.