Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the eye (HP:0000478)help
Parent Node:
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Abnormal eye physiology (HP:0012373)help
..Starting node
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Abnormal visual accommodation (HP:0030800)help
Term ID: 30800
Name: Abnormal visual accommodation
Synonym:
Definition: An anomaly in the process of visual accommodation, which is the process of adjustment of the eye to enable sharp vision of objects at different distances. Accommodation is mediated by contraction of the ciliary muscles, which alter the convexity of the lens and, consequently, its refractive power.
Comments:
Reference: HP:0030800
Genes and Diseases:
 
       Child Nodes:
........expandReduced visual accommodation (HP:0030801) help

 Sister Nodes: 
..expandAbnormal extraocular muscle physiology (HP:0025590) help
..expandAbnormal eyelid physiology (HP:0031879) help
..expandAbnormal intraocular pressure (HP:0012632) help
..expandAbnormal pupillary function (HP:0007686) help
..expandAbnormal visual electrophysiology (HP:0030453) help
..expandAbnormality of eye movement (HP:0000496) help
..expandAbnormality of refraction (HP:0000539) help
..expandAbnormality of vision (HP:0000504) help
..expandAsthenopia (HP:0031590) help
..expandCongenital stationary cone dysfunction (HP:0030637) help
..expandGlaucoma (HP:0000501) help
..expandHemorrhage of the eye (HP:0011885) help
..expandInflammatory abnormality of the eye (HP:0100533) help
..expandLacrimation abnormality (HP:0000632) help
..expandOcular pain (HP:0200026) help
..expandPtosis (HP:0000508) help
..expandStaring gaze (HP:0025401) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030800HP:0030800Abnormal visual accommodation0BAP1 CL E G H831439044ORPHA01191483950603089
HP:0030800HP:0030800Abnormal visual accommodation0CYSLTR2 CL E G H5710539044ORPHA026318274605666
HP:0030800HP:0030800Abnormal visual accommodation0GNA11 CL E G H276739044ORPHA0111284379139313
HP:0030800HP:0030800Abnormal visual accommodation0GNAQ CL E G H277639044ORPHA06724390600998
HP:0030800HP:0030800Abnormal visual accommodation0SF3B1 CL E G H2345139044ORPHA046710768605590
HP:0030800HP:0030800Abnormal visual accommodation1BAP1 CL E G H831439044ORPHA01191483950603089
HP:0030800HP:0030800Abnormal visual accommodation1CYSLTR2 CL E G H5710539044ORPHA026318274605666
HP:0030800HP:0030800Abnormal visual accommodation1GNA11 CL E G H276739044ORPHA0111284379139313
HP:0030800HP:0030800Abnormal visual accommodation1GNAQ CL E G H277639044ORPHA06724390600998
HP:0030800HP:0030800Abnormal visual accommodation1SF3B1 CL E G H2345139044ORPHA046710768605590


Genes (5) :BAP1 CYSLTR2 GNA11 GNAQ SF3B1

Diseases (1) :39044
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.