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222300
WFS1
WOLFRAM SYNDROME 1
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Musculoskeletal Diseases
Bone Diseases
Eosinophilic Granuloma
Digestive System Diseases
Gastrointestinal Diseases
Intestinal Diseases
Duodenal Diseases
Peptic Ulcer
Peptic Ulcer
Stomach Diseases
Peptic Ulcer
Respiratory Tract Diseases
Lung Diseases
Lung Diseases, Interstitial
Histiocytosis, Langerhans-Cell
Eosinophilic Granuloma
Pleural Diseases
Pneumothorax
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Deafness
Deaf-Blind Disorders
Wolfram Syndrome
Hearing Loss, Sensorineural
Nervous System Diseases
Autoimmune Diseases of the Nervous System
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Dysautonomia, Familial
Autonomic Nervous System Diseases
Primary Dysautonomias
Dysautonomia, Familial
Central Nervous System Diseases
Brain Diseases
Cerebellar Diseases
Cerebellar Ataxia
Spinocerebellar Ataxias
Ataxia Telangiectasia
Hypothalamic Diseases
Pituitary Diseases
Cranial Nerve Diseases
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Optic Atrophy, Autosomal Dominant
Wolfram Syndrome
Demyelinating Diseases
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Dysautonomia, Familial
Nervous System Malformations
Hereditary Sensory and Autonomic Neuropathies
Dysautonomia, Familial
Neurocutaneous Syndromes
Ataxia Telangiectasia
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Autonomic Neuropathies
Dysautonomia, Familial
Optic Atrophies, Hereditary
Optic Atrophy, Autosomal Dominant
Wolfram Syndrome
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Spinocerebellar Ataxias
Ataxia Telangiectasia
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Deaf-Blind Disorders
Wolfram Syndrome
Hearing Loss, Sensorineural
Vision Disorders
Blindness
Deaf-Blind Disorders
Wolfram Syndrome
Neuromuscular Diseases
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Autonomic Neuropathies
Dysautonomia, Familial
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Dysautonomia, Familial
Eye Diseases
Eye Abnormalities
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Optic Atrophy, Autosomal Dominant
Wolfram Syndrome
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Optic Atrophy, Autosomal Dominant
Wolfram Syndrome
Retinal Diseases
Diabetic Retinopathy
Vision Disorders
Blindness
Deaf-Blind Disorders
Wolfram Syndrome
Male Urogenital Diseases
Genital Diseases, Male
Testicular Diseases
Urologic Diseases
Kidney Diseases
Diabetes Insipidus
Wolfram Syndrome
Hydronephrosis
Ureteral Diseases
Urinary Bladder Diseases
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Diabetes Insipidus
Wolfram Syndrome
Hydronephrosis
Ureteral Diseases
Urinary Bladder Diseases
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
Heart Diseases
Heart Defects, Congenital
Myocardial Ischemia
Myocardial Infarction
Vascular Diseases
Diabetic Angiopathies
Diabetic Retinopathy
Hypertension
Myocardial Ischemia
Myocardial Infarction
Telangiectasis
Ataxia Telangiectasia
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Macrocytic
Anemia, Megaloblastic
Anemia, Sideroblastic
Bone Marrow Diseases
Myelodysplastic Syndromes
Anemia, Sideroblastic
Leukocyte Disorders
Eosinophilia
Eosinophilic Granuloma
Lymphatic Diseases
Histiocytosis
Histiocytosis, Langerhans-Cell
Eosinophilic Granuloma
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Deaf-Blind Disorders
Wolfram Syndrome
Wolfram Syndrome
Cardiovascular Abnormalities
Heart Defects, Congenital
Eye Abnormalities
Nervous System Malformations
Hereditary Sensory and Autonomic Neuropathies
Dysautonomia, Familial
Genetic Diseases, Inborn
Ataxia Telangiectasia
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Optic Atrophy, Autosomal Dominant
Wolfram Syndrome
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Autonomic Neuropathies
Dysautonomia, Familial
Optic Atrophies, Hereditary
Optic Atrophy, Autosomal Dominant
Wolfram Syndrome
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Cytochrome-c Oxidase Deficiency
Nutritional and Metabolic Diseases
Metabolic Diseases
DNA Repair-Deficiency Disorders
Ataxia Telangiectasia
Glucose Metabolism Disorders
Diabetes Mellitus
Diabetes Mellitus, Type 1
Wolfram Syndrome
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Mitochondrial Diseases
Cytochrome-c Oxidase Deficiency
Optic Atrophy, Autosomal Dominant
Nutrition Disorders
Malnutrition
Deficiency Diseases
Avitaminosis
Vitamin B Deficiency
Thiamine Deficiency
Endocrine System Diseases
Diabetes Mellitus
Diabetes Complications
Diabetic Angiopathies
Diabetic Retinopathy
Diabetes Mellitus, Type 1
Wolfram Syndrome
Gonadal Disorders
Hypogonadism
Testicular Diseases
Pituitary Diseases
Diabetes Insipidus
Wolfram Syndrome
Immune System Diseases
Autoimmune Diseases
Autoimmune Diseases of the Nervous System
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Dysautonomia, Familial
Diabetes Mellitus, Type 1
Immunologic Deficiency Syndromes
Ataxia Telangiectasia
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Pathologic Processes
Disease
Syndrome
Disease Attributes
Chronic Disease
Disease Susceptibility
Genetic Predisposition to Disease
Diseases in Twins
Granuloma
Eosinophilic Granuloma
Postoperative Complications
Signs and Symptoms
Neurologic Manifestations
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Hearing Loss, Sensorineural
Vision Disorders
Blindness
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