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312700
RS1
RETINOSCHISIS 1, X-LINKED, JUVENILE
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Neoplasms
Neoplasms by Histologic Type
Neoplasms, Germ Cell and Embryonal
Neuroectodermal Tumors
Neoplasms, Neuroepithelial
Retinoblastoma
Neoplasms, Glandular and Epithelial
Neoplasms, Neuroepithelial
Retinoblastoma
Neoplasms, Nerve Tissue
Neuroectodermal Tumors
Neoplasms, Neuroepithelial
Retinoblastoma
Neoplasms by Site
Eye Neoplasms
Retinal Neoplasms
Retinoblastoma
Nervous System Diseases
Cranial Nerve Diseases
Ocular Motility Disorders
Nystagmus, Pathologic
Strabismus
Neurologic Manifestations
Sensation Disorders
Vision Disorders
Blindness
Color Vision Defects
Eye Diseases
Eye Diseases, Hereditary
Eye Neoplasms
Retinal Neoplasms
Retinoblastoma
Ocular Hypertension
Glaucoma
Glaucoma, Neovascular
Ocular Motility Disorders
Nystagmus, Pathologic
Strabismus
Refractive Errors
Hyperopia
Retinal Diseases
Retinal Degeneration
Macular Degeneration
Retinoschisis
Retinal Detachment
Retinal Neoplasms
Retinoblastoma
Retinal Perforations
Vision Disorders
Blindness
Color Vision Defects
Male Urogenital Diseases
Urologic Diseases
Kidney Diseases
Renal Tubular Transport, Inborn Errors
Hypophosphatemia, Familial
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Renal Tubular Transport, Inborn Errors
Hypophosphatemia, Familial
Pregnancy Complications
Abortion, Spontaneous
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Coagulation Disorders
Blood Coagulation Disorders, Inherited
Hemophilia A
Coagulation Protein Disorders
Hemophilia A
Hemorrhagic Disorders
Hemophilia A
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Genetic Diseases, Inborn
Blood Coagulation Disorders, Inherited
Hemophilia A
Eye Diseases, Hereditary
Genetic Diseases, X-Linked
Metabolism, Inborn Errors
Metal Metabolism, Inborn Errors
Hypophosphatemia, Familial
Renal Tubular Transport, Inborn Errors
Hypophosphatemia, Familial
Skin Diseases, Genetic
Darier Disease
Skin and Connective Tissue Diseases
Skin Diseases
Keratosis
Darier Disease
Skin Diseases, Genetic
Darier Disease
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Metal Metabolism, Inborn Errors
Hypophosphatemia, Familial
Renal Tubular Transport, Inborn Errors
Hypophosphatemia, Familial
Phosphorus Metabolism Disorders
Hypophosphatemia
Hypophosphatemia, Familial
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Sex Chromosome Aberrations
Disease
Syndrome
Disease Attributes
Disease Progression
Signs and Symptoms
Neurologic Manifestations
Sensation Disorders
Vision Disorders
Blindness
Color Vision Defects
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