Human Phenotype Ontology 
Grandparent Node:
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Abnormal retinal morphology (HP:0000479)help
Grandparent Node:
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Coloboma (HP:0000589)help
Parent Node:
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Retinal coloboma (HP:0000480)help
..Starting node
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obsolete Bilateral retinal coloboma (HP:0007808)help
Term ID: 7808
Name: obsolete Bilateral retinal coloboma
Synonym:
Definition:
Comments:
Reference: HP:0007808
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandInferior retinal coloboma (HP:0031614) help
..expandMacular coloboma (HP:0001116) 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:0007808HP:0007808obsolete Bilateral retinal coloboma0 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.