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
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Mild myopia (HP:0025573)help
Term ID: 25573
Name: Mild myopia
Synonym:
Definition: A mild form of myopia with up to -3.00 diopters.
Comments:
Reference: HP:0025573
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAxial myopia (HP:0031730) help
..expandHigh myopia (HP:0011003) help
..expandLatent myopia (HP:0500066) help
..expandModerate myopia (HP:0031624) help
..expandobsolete Congenital myopia (HP:0008012) 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:0025573HP:0025573Mild myopia0AHDC1 CL E G H2724525230ORPHA:412069AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndromeHP:0040283 - Occasional36
HP:0025573HP:0025573Mild myopia0COL11A2 CL E G H13022187ORPHA:1427Otospondylomegaepiphyseal dysplasiaHP:0040284 - Very rare222
HP:0025573HP:0025573Mild myopia0GNB3 CL E G H27844400OMIM:617024Night blindness, congenital stationary, type 1H.5
HP:0025573HP:0025573Mild myopia0H4C5 CL E G H83674790OMIM:619950
HP:0025573HP:0025573Mild myopia0OFD1 CL E G H84812567OMIM:300424Retinitis pigmentosa 23201
HP:0025573HP:0025573Mild myopia0POGZ CL E G H2312618801OMIM:616364White-Sutton syndrome35


Genes (6) :AHDC1 COL11A2 GNB3 H4C5 OFD1 POGZ

Diseases (6) :ORPHA:412069 ORPHA:1427 OMIM:617024 OMIM:619950 OMIM:300424 OMIM:616364
 

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