Human Phenotype Ontology 
Grandparent Node:
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Abnormality of refraction (HP:0000539)help
Parent Node:
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Myopia (HP:0000545)help
..Starting node
..expand
obsolete Congenital myopia (HP:0008012)help
Term ID: 8012
Name: obsolete Congenital myopia
Synonym:
Definition:
Comments:
Reference: HP:0008012
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAxial myopia (HP:0031730) help
..expandHigh myopia (HP:0011003) help
..expandLatent myopia (HP:0500066) help
..expandMild myopia (HP:0025573) help
..expandModerate myopia (HP:0031624) 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:0008012HP:0008012obsolete Congenital myopia0 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.