MeSH Treeview
Query OMIM entry list
266920
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RENAL DYSPLASIA, RETINAL PIGMENTARY DYSTROPHY, CEREBELLAR ATAXIA, AND SKELETAL DYSPLASIA
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Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Digestive System Diseases
Liver Diseases
Liver Cirrhosis
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Cerebellar Diseases
Cerebellar Ataxia
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Eye Diseases
Eye Diseases, Hereditary
Retinitis Pigmentosa
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Male Urogenital Diseases
Urologic Diseases
Kidney Diseases
Fanconi Syndrome
Renal Tubular Transport, Inborn Errors
Fanconi Syndrome
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Fanconi Syndrome
Renal Tubular Transport, Inborn Errors
Fanconi Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Retinitis Pigmentosa
Metabolism, Inborn Errors
Renal Tubular Transport, Inborn Errors
Fanconi Syndrome
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Renal Tubular Transport, Inborn Errors
Fanconi Syndrome
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease
Syndrome
Ossification, Heterotopic
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Database Center for Life Science
