Optic AtrophyOptic Atrophy, Autosomal DominantOptic Atrophies, HereditaryOptic Atrophy, Hereditary, LeberLeber Congenital AmaurosisAtrophyOptic NerveWolfram SyndromePressureOptic DiskGTP PhosphohydrolasesBlood PressureBlindnessMuscular AtrophyOptic Neuritiscis-trans-IsomerasesPedigreeHereditary Sensory and Motor NeuropathyOptic ChiasmDNA, MitochondrialRetinal Ganglion CellsPapilledemaVision DisordersVisual AcuityElectroretinographyOptic Nerve InjuriesHydrostatic PressureRetinaMuscular Atrophy, SpinalMutationDNA Mutational AnalysisEye ProteinsGenes, RecessiveEye DiseasesOnchocerciasis, OcularMitochondrial DiseasesIntraocular PressureNADH DehydrogenaseMultiple System AtrophyOptic Neuropathy, IschemicRetinal DegenerationOptic Lobe, NonmammalianBlood Pressure DeterminationGlutaratesVisual FieldsOptic FlowFundus OculiConsanguinityMutation, MissenseDiabetes InsipidusCodon, NonsenseSyndromeMitochondrial DynamicsMyoclonic Cerebellar DyssynergiaVision, LowMitochondrial ProteinsSpinal Muscular Atrophies of ChildhoodMitochondriaRetinal DiseasesIntracranial PressureOptics and PhotonicsNerve FibersDisease Models, AnimalMicrocephalyPhotoreceptor Connecting CiliumTransducers, PressureHypertensionCerebellar AtaxiaMagnetic Resonance ImagingColor Vision DefectsOptic Nerve GliomaEvoked Potentials, VisualRetinitis PigmentosaPhenotypeBlood Pressure Monitoring, AmbulatoryRetinal DystrophiesOptic Nerve DiseasesTomography, Optical CoherenceGenetic LinkageAir PressureMolecular Sequence DataAtmospheric PressureOlivopontocerebellar AtrophiesGenetic HeterogeneityHomozygoteVenous PressureMembrane ProteinsPhotoreceptor Cells, VertebrateLeigh DiseaseVisual Field TestsGyrate AtrophyDeafnessPenetranceEye Diseases, HereditaryGenes, DominantGlaucomaHearing Loss, SensorineuralChromosomes, Human, Pair 3Arterial PressureHaplotypes