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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Eye Diseases (D005128)
..Starting node ..Ocular Hypertension (D009798)
Child Nodes:
........Glaucoma (D005901) 51
Sister Nodes:
..Asthenopia (D001248)
..Cogan Syndrome (D055952) 2
..Conjunctival Diseases (D003229) 29
..Corneal Diseases (D003316) 120
..Encephalocraniocutaneous lipomatosis (C535736)
..Exudative Vitreoretinopathy 4 (C566619)
..Exudative Vitreoretinopathy 5 (C567648)
..Eye Abnormalities (D005124) 208
..Eye Diseases, Hereditary (D015785) 373
..Eye Hemorrhage (D005130) 6
..Eye Infections (D015817) 25
..Eye Injuries (D005131) 7
..Eye Manifestations (D005132) 9
..Eye Neoplasms (D005134) 20
..Eyelid Diseases (D005141) 64
..Hernandez Fragoso syndrome (C536062)
..Lacrimal Apparatus Diseases (D007766) 18
..Lens Diseases (D007905) 166
..Mollica Pavone Antener syndrome (C535809)
..MORM syndrome (C536984)
..Neuropathy, Hereditary Sensorimotor, with Upper Motor Neuron, Visual Pathway and Autonomic Disturbance (C563517)
..Ocular Hypertension (D009798) 52
..Ocular Hypotension (D015814)
..Ocular Motility Disorders (D015835) 109
..Optic Nerve Diseases (D009901) 69
..Orbital Diseases (D009916) 17
..Pupil Disorders (D011681) 20
..Refractive Errors (D012030) 57
..Retinal Diseases (D012164) 287
..Scleral Diseases (D015422) 3
..Uveal Diseases (D014603) 59
..Vision Disorders (D014786) 84
..Vitreoretinopathy, Proliferative (D018630) 5
..Vitreous Detachment (D020255) 1
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8168
Name:	Ocular Hypertension
Definition:	A condition in which the intraocular pressure is elevated above normal and which may lead to glaucoma.
Alternative IDs:
ParentIDs:	MESH:D005128
TreeNumbers:	C11.525
Synonyms:	Glaucomas, Suspect \|Glaucoma, Suspect \|Hypertension, Ocular \|Hypertensions, Ocular \|Ocular Hypertensions \|Suspect Glaucoma \|Suspect Glaucomas
Slim Mappings:	Eye disease
Reference:	MedGen: D009798 MeSH: D009798 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants