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611536
MAFD6
MAJOR AFFECTIVE DISORDER 6
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Digestive System Diseases
Gastrointestinal Diseases
Esophageal Diseases
Deglutition Disorders
Respiratory Tract Diseases
Respiration Disorders
Respiratory Insufficiency
Airway Obstruction
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Deafness
Deaf-Blind Disorders
Wolfram Syndrome
Pharyngeal Diseases
Deglutition Disorders
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Huntington Disease
Cerebellar Diseases
Cerebellar Ataxia
Spinocerebellar Ataxias
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Dementia
Huntington Disease
Movement Disorders
Dyskinesias
Chorea
Huntington Disease
Spinal Cord Diseases
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Cranial Nerve Diseases
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Wolfram Syndrome
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Huntington Disease
Optic Atrophies, Hereditary
Wolfram Syndrome
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Spinocerebellar Ataxias
Neurobehavioral Manifestations
Memory Disorders
Intellectual Disability
Psychomotor Disorders
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Deaf-Blind Disorders
Wolfram Syndrome
Vision Disorders
Blindness
Deaf-Blind Disorders
Wolfram Syndrome
Eye Diseases
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Wolfram Syndrome
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Wolfram Syndrome
Vision Disorders
Blindness
Deaf-Blind Disorders
Wolfram Syndrome
Male Urogenital Diseases
Urologic Diseases
Kidney Diseases
Diabetes Insipidus
Wolfram Syndrome
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Diabetes Insipidus
Wolfram Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Deaf-Blind Disorders
Wolfram Syndrome
Wolfram Syndrome
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Wolfram Syndrome
Heredodegenerative Disorders, Nervous System
Huntington Disease
Optic Atrophies, Hereditary
Wolfram Syndrome
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Nutritional and Metabolic Diseases
Metabolic Diseases
Glucose Metabolism Disorders
Diabetes Mellitus
Diabetes Mellitus, Type 1
Wolfram Syndrome
Endocrine System Diseases
Diabetes Mellitus
Diabetes Mellitus, Type 1
Wolfram Syndrome
Pituitary Diseases
Diabetes Insipidus
Wolfram Syndrome
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Translocation, Genetic
Disease
Syndrome
Disease Attributes
Acute Disease
Chronic Disease
Disease Susceptibility
Genetic Predisposition to Disease
Anticipation, Genetic
Recurrence
Growth Disorders
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Memory Disorders
Intellectual Disability
Psychomotor Disorders
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