Cone-Rod Dystrophy 2
|
Bardet-Biedl Syndrome
|
Retinal Degeneration
|
Liver Cirrhosis, Experimental
|
Csnb1c
|
Melanoma
|
Cataract
|
Craniofacial Abnormalities
|
Colorectal Cancer
|
Autism
|
Breast Carcinoma
|
Leber Congenital Amaurosis
|
Myopia
|
Intellectual Disability
|
Abortion, Spontaneous
|
Retinal Dystrophies
|
Autoimmune Disease
|
Disease Models, Animal
|
Fundus Albipunctatus
|
Uveitis
|
Inflammation
|
Cataract, Autosomal Dominant
|
Stomach Neoplasms
|
Prostatic Neoplasms
|
Drug Dependence
|
Basal Cell Carcinoma
|
Mammary Neoplasms, Animal
|
Carcinoma
|
Endometriosis
|
Age-Related Macular Degeneration
|
Mammary Neoplasms, Experimental
|
Color Vision Defects
|
Eye Diseases, Hereditary
|
Acute Lymphoblastic Leukemia
|
Liver Diseases
|
Polycystic Ovary Syndrome
|
Cataract, Coppock-Like
|
Hyperexplexia Hereditary
|
Lung Neoplasms
|
Oguchi Disease
|
Diabetes Mellitus, Type 2
|
Small Cell Lung Carcinoma
|
Optic Atrophy, Hereditary, Leber
|
Stargardt Disease 1
|
Osteoarthritis
|
Weight Loss
|
Osteochondrodysplasias
|
Hypertension
|
Calcinosis
|
Glaucoma, Primary Open Angle
|
Drug-Induced Liver Injury
|
Hepatocellular Carcinoma
|
Ovarian Cysts
|
Usher Syndromes
|
Usher Syndrome, Type 1d
|
Pancreatic Carcinoma
|
Mouth Neoplasms
|
Dyskinesia, Drug-Induced
|
Peters Anomaly
|
Vision Disorders
|
Squamous Cell Carcinoma
|
Attention Deficit Hyperactivity Disorder
|
Hearing Loss, Sensorineural
|
Blue Cone Monochromatism
|
Nerve Degeneration
|
Reflex, Abnormal
|
Vitamin A Deficiency
|
Best Vitelliform Macular Dystrophy, Multifocal
|
Neoplasm Invasiveness
|
Neural Tube Defects
|
Anxiety Disorder
|
Neurotoxicity Syndromes
|
Heart Valve Diseases
|
Prolonged Electroretinal Response Suppression
|
Leber Congenital Amaurosis 3
|
Brain Diseases
|
Asthma
|
Liver Cirrhosis
|
Cone-Rod Dystrophy, X-Linked, 3
|
Corneal Dystrophies, Hereditary
|
Corneal Dystrophy Avellino Type
|
Corneal Dystrophy, Epithelial Basement Membrane
|
Corneal Dystrophy, Gelatinous Drop-Like
|
Corneal Dystrophy, Juvenile Epithelial Of Meesmann
|
Corneal Dystrophy, Lattice Type Iiia
|
Corneal Dystrophy Of Bowman Layer, Type 1
|
Corneal Dystrophy, Posterior Polymorphous, 1
|
Corneal Dystrophy, Thiel-Behnke Type
|
Cornea Plana 2
|
Costeff Optic Atrophy Syndrome
|
Craniosynostoses
|
Creutzfeldt Jacob Disease
|
Deafness
|
Deafness, Autosomal Dominant 10
|
Deafness, Autosomal Dominant 11
|
Deafness, Autosomal Dominant 15
|
Deafness, Autosomal Dominant 6
|
Deafness, Autosomal Recessive 12
|
Deafness, Autosomal Recessive 2
|
Deafness, Autosomal Recessive 23
|
Deafness, Autosomal Recessive 30
|
Dermatitis, Contact
|
Diabetes Mellitus, Experimental
|
Diabetic Nephropathy
|
Disease Progression
|
Doyne Honeycomb Retinal Dystrophy
|
Limb Dystonia
|
Dystonic Disorders
|
Ectodermal Dysplasia, Ectrodactyly, And Macular Dystrophy
|
Ectopia Pupillae
|
Edema
|
Ehlers-Danlos Syndrome Type 1
|
Ehlers-Danlos Syndrome, Type Vii, Autosomal Dominant
|
Empty Sella Syndrome
|
Enhanced S-Cone Syndrome
|
Enterocolitis, Necrotizing
|
Epilepsy
|
Epilepsy, Female-Restricted, With Mental Retardation
|
Epilepsy, Frontal Lobe
|
Epilepsy, Nocturnal Frontal Lobe, Type 3
|
Epiphyseal Dysplasia, Multiple, With Myopia And Conductive Deafness
|
Erythema
|
Erythrocytosis, Familial, 4
|
Esophageal Squamous Cell Carcinoma
|
Eye Abnormalities
|
Febrile Convulsions, Familial, 4
|
Female Urogenital Diseases
|
Femur Head Necrosis
|
Fibrosis
|
Fractures, Bone
|
Fundus Dystrophy, Pseudoinflammatory, Of Sorsby
|
Gait Ataxia
|
Glaucoma 1, Open Angle, A
|
Glaucoma 1, Open Angle, G
|
Glaucoma 3, Primary Congenital, A
|
Glaucoma, Angle-Closure
|
Gliosis
|
Griscelli Syndrome Type 1
|
Groenouw Type I Corneal Dystrophy
|
Gyrate Atrophy
|
Hearing Loss
|
Heart Defects, Congenital
|
Heart Diseases
|
Heart Failure
|
Hemangiosarcoma
|
Heredodegenerative Disorders, Nervous System
|
Cyclopia
|
Holoprosencephaly 2
|
Holoprosencephaly 5
|
Hyaloideoretinal Degeneration Of Wagner
|
Hyperkinesis
|
Hyperlipoproteinemia Type Iv
|
Hyperostosis, Cortical, Congenital
|
Hyperplasia
|
Left Ventricular Hypertrophy
|
Hypomagnesemia 5, Renal, With Ocular Involvement
|
Hypothermia
|
Male Infertility
|
Intervertebral Disc Disease
|
Intervertebral Disc Displacement
|
Juvenile Macular Degeneration And Hypotrichosis
|
Keloid
|
Keratitis, Hereditary
|
Keratoconus
|
Keratoconus 1
|
Keratomalacia
|
Kidney Disease
|
Kidney Failure, Chronic
|
Kniest Dysplasia
|
Knobloch Syndrome
|
Lacrimal Apparatus Diseases
|
Lattice Corneal Dystrophy Type 1
|
Learning Disorders
|
Leber Congenital Amaurosis 12
|
Leber Congenital Amaurosis 13
|
Leber Congenital Amaurosis 14
|
Leber Congenital Amaurosis 4
|
Legg-Calve-Perthes Disease
|
Liver Diseases, Alcoholic
|
Liver Neoplasms
|
Liver Neoplasms, Experimental
|
Lung Diseases
|
Macular Degeneration, Age-Related, 1
|
Macular Degeneration, Age-Related, 2
|
Macular Dystrophy, Concentric Annular
|
Marshall Syndrome
|
Mckusick Kaufman Syndrome
|
Megaepiphyseal Dwarfism
|
Mental Retardation, X-Linked
|
Mesangial Sclerosis, Diffuse
|
Mesothelioma, Malignant
|
Microphthalmia, Isolated 2
|
Microphthalmia, Isolated 3
|
Microphthalmia, Isolated, With Cataract 2
|
Microphthalmia, Isolated, With Coloboma 3
|
Motor Skills Disorders
|
Movement Disorder
|
Multiple Sclerosis
|
Muscular Dystrophy, Facioscapulohumeral
|
Myoclonic Epilepsies, Progressive
|
Nanophthalmos 2
|
Necrosis
|
Neoplasm Metastasis
|
Neoplasms, Experimental
|
Nephrogenic Fibrosing Dermopathy
|
Nephronophthisis 3
|
Nephrotic Syndrome
|
Nervous System Malformations
|
Neuroblastoma
|
Neuronal Ceroid-Lipofuscinoses
|
Newfoundland Rod-Cone Dystrophy
|
Night Blindness
|
Night Blindness, Congenital Stationary, Autosomal Dominant 1
|
Night Blindness, Congenital Stationary, Autosomal Dominant 2
|
Night Blindness, Congenital Stationary, Autosomal Dominant 3
|
Norrie Disease
|
Nystagmus, Congenital
|
Nystagmus, Pathologic
|
Ocular Albinism Type 1
|
Oculocutaneous Albinism Type 1
|
Oculocutaneous Albinism Type 1b
|
Oculocutaneous Albinism, Type Iv
|
O'Donnell Pappas Syndrome
|
Optic Atrophy 1 And Deafness
|
Optic Atrophy And Cataract, Autosomal Dominant
|
Optic Atrophy, Autosomal Dominant
|
Optic Nerve Diseases
|
Optic Nerve Hypoplasia, Bilateral
|
Oral Submucous Fibrosis
|
Osteoarthritis With Mild Chondrodysplasia
|
Osteogenesis Imperfecta
|
Osteogenesis Imperfecta, Type 2a
|
Osteogenesis Imperfecta, Type 3
|
Osteogenesis Imperfecta, Type 4
|
Osteoporosis
|
Osteosarcoma
|
Ovarian Neoplasms
|
Papillorenal Syndrome
|
Parkinsonian Disorders
|
Patterned Dystrophy Of Retinal Pigment Epithelium
|
Peripheral Neuropathy
|
Pheochromocytoma
|
Photophobia
|
Pierson Syndrome
|
Platyspondylic Lethal Skeletal Dysplasia, Torrance Type
|
Pneumoconiosis
|
Polycystic Kidney, Autosomal Recessive
|
Precancerous Conditions
|
Pseudoxanthoma Elasticum
|
Psychoses, Substance-Induced
|
Refractive Errors
|
Renal Hepatic Pancreatic Dysplasia Dandy Walker Cyst
|
Respiratory Tract Infections
|
Retinal Cone Dystrophy 2
|
Retinal Cone Dystrophy 3a
|
Retinal Detachment
|
Retinal Diseases
|
Retinitis Pigmentosa 1
|
Retinitis Pigmentosa 14
|
Retinitis Pigmentosa 19
|
Retinitis Pigmentosa 2
|
Retinitis Pigmentosa 3
|
Retinitis Pigmentosa 30
|
Retinitis Pigmentosa 36
|
Retinitis Pigmentosa 37
|
Retinitis Pigmentosa 4
|
Retinitis Pigmentosa 7
|
Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness
|
Retinoblastoma
|
Retinoschisis
|
Schistosomiasis
|
Schizophrenia
|
Scrapie
|
Segawa Syndrome, Autosomal Recessive
|
Sesame Syndrome
|
Sezary Syndrome
|
Skin Diseases
|
Skin Neoplasms
|
Sleep Wake Disorders
|
Spinocerebellar Ataxias
|
Spondyloepiphyseal Dysplasia, Congenita
|
Spondylometaphyseal Dysplasia, Kozlowski Type
|
Toxic Epidermal Necrolysis
|
Stickler Syndrome, Type 1
|
Stickler Syndrome, Type 2
|
Stickler Syndrome, Type I, Nonsyndromic Ocular
|
Strudwick Syndrome
|
Substance Withdrawal Syndrome
|
Sudden Infant Death
|
Synovitis
|
Tooth Abnormalities
|
Urinary Bladder Diseases
|
Urinary Bladder Neoplasms
|
Usher Syndrome, Type 1b
|
Usher Syndrome, Type 1f
|
Usher Syndrome, Type 2a
|
Usher Syndrome, Type 2c
|
Vitreoretinochoroidopathy
|
Wolfram Syndrome
|
3-Methylglutaconic Aciduria, Type V
|
Wounds And Injuries
|
Achondrogenesis Type 2
|
Achromatopsia 2
|
Achromatopsia 3
|
Adenocarcinoma
|
Adenoma
|
Adrenal Gland Neoplasms
|
Adrenocortical Carcinoma
|
Aland Island Eye Disease
|
Albinism Ocular Late Onset Sensorineural Deafness
|
Albinism, Oculocutaneous
|
Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial Cells
|
Alzheimer's Disease
|
Amaurosis Congenita Of Leber, Type 1
|
Amaurosis Congenita Of Leber, Type 2
|
Amaurosis Hypertrichosis
|
Amphetamine-Related Disorders
|
Anemia, Hypochromic Microcytic
|
Aneurysm, Dissecting
|
Aniridia
|
Aniridia Cerebellar Ataxia Mental Deficiency
|
Aniridia, Type 2
|
Anodontia
|
Anophthalmos
|
Aortic Valve Insufficiency
|
Arsenic Poisoning
|
Arthritis
|
Arthritis, Experimental
|
Asbestosis
|
Atrophy
|
Auditory Perceptual Disorders
|
Autism Spectrum Disorder
|
Bietti Crystalline Dystrophy
|
Blindness
|
Bothnia Retinal Dystrophy
|
Brain Injuries
|
Brain Ischemia
|
Brugada Syndrome 4
|
Carcinoma, Non-Small-Cell Lung
|
Renal Cell Carcinoma
|
Cardiac Hypertrophy
|
Cardiomyopathy, Dilated, 1j
|
Catalepsy
|
Cataract, Autosomal Dominant, Multiple Types 1
|
Cataract, Congenital Nuclear, Autosomal Recessive 2
|
Cataract, Congenital Nuclear, Autosomal Recessive 3
|
Cataract, Congenital Zonular, With Sutural Opacities
|
Cataract Microcornea Syndrome
|
Cataract, Zonular
|
Cataract, Zonular Pulverulent 1
|
Cataract, Zonular Pulverulent 3
|
Cell Transformation, Neoplastic
|
Ceroid Lipofuscinosis, Neuronal, 1
|
Ceroid Lipofuscinosis, Neuronal 1, Infantile
|
Ceroid Lipofuscinosis, Neuronal 5
|
Ceroid Lipofuscinosis, Neuronal, 6
|
Ceroid Lipofuscinosis, Neuronal 8
|
Cerulean Cataract
|
Cholangitis
|
Chondrosarcoma
|
Chordoma
|
Choroidal Dystrophy, Central Areolar 2
|
Choroideremia
|
Chromosome Aberrations
|
Chromosome Xp11.3 Deletion Syndrome
|
Cleft Lip
|
Cochlear Diseases
|
Colitis
|
Ulcerative Colitis
|
Coloboma
|
Coloboma Of Optic Nerve
|
Cone Dystrophy 3
|
Cone Dystrophy 4
|
Cone-Rod Dystrophy 11
|
Cone-Rod Dystrophy 13
|
Cone-Rod Dystrophy 3
|
Cone-Rod Dystrophy 5
|
Cone-Rod Dystrophy 7
|