MeSH Treeview
Query OMIM entry list
557000
-
PEARSON MARROW-PANCREAS SYNDROME
→
High-scoring List
Musculoskeletal Diseases
Muscular Diseases
Mitochondrial Myopathies
Ophthalmoplegia, Chronic Progressive External
Kearns-Sayre Syndrome
Digestive System Diseases
Pancreatic Diseases
Exocrine Pancreatic Insufficiency
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Cranial Nerve Diseases
Ocular Motility Disorders
Ophthalmoplegia
Ophthalmoplegia, Chronic Progressive External
Ophthalmoplegia, Chronic Progressive External
Kearns-Sayre Syndrome
Neurologic Manifestations
Paralysis
Ophthalmoplegia
Ophthalmoplegia, Chronic Progressive External
Neuromuscular Diseases
Muscular Diseases
Mitochondrial Myopathies
Ophthalmoplegia, Chronic Progressive External
Kearns-Sayre Syndrome
Eye Diseases
Eye Diseases, Hereditary
Retinitis Pigmentosa
Lens Diseases
Cataract
Ocular Motility Disorders
Ophthalmoplegia
Ophthalmoplegia, Chronic Progressive External
Ophthalmoplegia, Chronic Progressive External
Kearns-Sayre Syndrome
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Kearns-Sayre Syndrome
Male Urogenital Diseases
Urologic Diseases
Kidney Diseases
Fanconi Syndrome
Renal Tubular Transport, Inborn Errors
Fanconi Syndrome
Renal Aminoacidurias
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Fanconi Syndrome
Renal Tubular Transport, Inborn Errors
Fanconi Syndrome
Renal Aminoacidurias
Cardiovascular Diseases
Heart Diseases
Cardiomyopathies
Kearns-Sayre Syndrome
Ventricular Dysfunction
Ventricular Dysfunction, Left
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Aplastic
Anemia, Hypoplastic, Congenital
Fanconi Anemia
Anemia, Sideroblastic
Blood Platelet Disorders
Thrombocytopenia
Bone Marrow Diseases
Anemia, Aplastic
Anemia, Hypoplastic, Congenital
Fanconi Anemia
Myelodysplastic Syndromes
Anemia, Sideroblastic
Leukocyte Disorders
Leukopenia
Agranulocytosis
Neutropenia
Pancytopenia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Anemia, Hypoplastic, Congenital
Fanconi Anemia
Eye Diseases, Hereditary
Retinitis Pigmentosa
Metabolism, Inborn Errors
Renal Tubular Transport, Inborn Errors
Fanconi Syndrome
Renal Aminoacidurias
Infant, Newborn, Diseases
Nutritional and Metabolic Diseases
Metabolic Diseases
Acid-Base Imbalance
Acidosis
Acidosis, Lactic
DNA Repair-Deficiency Disorders
Fanconi Anemia
Glucose Metabolism Disorders
Diabetes Mellitus
Diabetes Mellitus, Type 1
Metabolism, Inborn Errors
Renal Tubular Transport, Inborn Errors
Fanconi Syndrome
Renal Aminoacidurias
Mitochondrial Diseases
Kearns-Sayre Syndrome
Mitochondrial Myopathies
Ophthalmoplegia, Chronic Progressive External
Kearns-Sayre Syndrome
Endocrine System Diseases
Diabetes Mellitus
Diabetes Complications
Diabetes Mellitus, Type 1
Immune System Diseases
Autoimmune Diseases
Diabetes Mellitus, Type 1
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Disease
Syndrome
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Fibrosis
Growth Disorders
Signs and Symptoms
Neurologic Manifestations
Paralysis
Ophthalmoplegia
Ophthalmoplegia, Chronic Progressive External
Database Center for Life Science
