Human Phenotype Ontology 
Grandparent Node:
expandAbnormal ocular adnexa morphology (HP:0030669)help
Parent Node:
expandAbnormal conjunctiva morphology (HP:0000502)help
..Starting node
..expandDefect of palpebral conjunctiva (HP:0430011)help
Term ID: 430011
Name: Defect of palpebral conjunctiva
Synonym:
Definition: An abnormality of the palpebral conjunctiva.
Comments:
Reference: HP:0430011
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal morphology of the conjunctival vasculature (HP:0008054) help
..expandBitot spots of the conjunctiva (HP:0007462) 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
..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:0430011HP:0430011Defect of palpebral 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.