Human Phenotype Ontology 
Grandparent Node:
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Glaucoma (HP:0000501)help
Parent Node:
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Developmental glaucoma (HP:0001087)help
..Starting node
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Late onset congenital glaucoma (HP:0008041)help
Term ID: 8041
Name: Late onset congenital glaucoma
Synonym:
Definition:
Comments:
Reference: HP:0008041
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBuphthalmos (HP:0000557) help
..expandPrimary congenital glaucoma (HP:0008007) 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:0008041HP:0008041Late onset congenital glaucoma0CYP1B1 CL E G H15452597OMIM:231300Glaucoma 3, primary congenital, A.101


Genes (1) :CYP1B1

Diseases (1) :OMIM:231300
 

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