Human Phenotype Ontology 
Grandparent Node:
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Abnormality of vision (HP:0000504)help
Parent Node:
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Visual loss (HP:0000572)help
..Starting node
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Nonprogressive visual loss (HP:0200068)help
Term ID: 200068
Name: Nonprogressive visual loss
Synonym: Decreased visual acuity, nonprogressive
Definition:
Comments:
Reference: HP:0200068
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandProgressive visual loss (HP:0000529) 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:0200068HP:0200068Nonprogressive visual loss0BTD CL E G H6861122ORPHA:79241Biotinidase deficiencyHP:0040283 - Occasional223
HP:0200068HP:0200068Nonprogressive visual loss0NBAS CL E G H5159415625OMIM:614800Short stature, optic nerve atrophy, and pelger-huet anomaly.25


Genes (2) :BTD NBAS

Diseases (2) :ORPHA:79241 OMIM:614800
 

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