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216400
CSA
COCKAYNE SYNDROME, TYPE A
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Neoplasms
Precancerous Conditions
Xeroderma Pigmentosum
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dwarfism
Cockayne Syndrome
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Digestive System Diseases
Liver Diseases
alpha 1-Antitrypsin Deficiency
Stomatognathic Diseases
Tooth Diseases
Tooth Demineralization
Dental Caries
Respiratory Tract Diseases
Lung Diseases
alpha 1-Antitrypsin Deficiency
Hypertension, Pulmonary
Pulmonary Emphysema
Respiration Disorders
Respiratory Insufficiency
Airway Obstruction
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Deafness
Hearing Loss, Sensorineural
Nervous System Diseases
Autoimmune Diseases of the Nervous System
Demyelinating Autoimmune Diseases, CNS
Diffuse Cerebral Sclerosis of Schilder
Central Nervous System Diseases
Brain Diseases
Dementia
Diffuse Cerebral Sclerosis of Schilder
Hydrocephalus
Hydrocephalus, Normal Pressure
Intracranial Hypertension
Hydrocephalus
Leukoencephalopathies
Demyelinating Autoimmune Diseases, CNS
Diffuse Cerebral Sclerosis of Schilder
Leukoencephalopathies
Demyelinating Autoimmune Diseases, CNS
Diffuse Cerebral Sclerosis of Schilder
Movement Disorders
Cranial Nerve Diseases
Ocular Motility Disorders
Nystagmus, Pathologic
Strabismus
Demyelinating Diseases
Demyelinating Autoimmune Diseases, CNS
Diffuse Cerebral Sclerosis of Schilder
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Cockayne Syndrome
Neurologic Manifestations
Dyskinesias
Ataxia
Neurobehavioral Manifestations
Intellectual Disability
Reflex, Abnormal
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Hearing Loss, Sensorineural
Vision Disorders
Neuromuscular Diseases
Peripheral Nervous System Diseases
Eye Diseases
Corneal Diseases
Corneal Opacity
Eye Diseases, Hereditary
Retinitis Pigmentosa
Lens Diseases
Cataract
Ocular Motility Disorders
Nystagmus, Pathologic
Strabismus
Orbital Diseases
Enophthalmos
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Vision Disorders
Male Urogenital Diseases
Urologic Diseases
Kidney Diseases
Nephritis
Glomerulonephritis
Glomerulosclerosis, Focal Segmental
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Nephritis
Glomerulonephritis
Glomerulosclerosis, Focal Segmental
Pregnancy Complications
Fetal Diseases
Cardiovascular Diseases
Vascular Diseases
Hypertension
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Aplastic
Anemia, Hypoplastic, Congenital
Fanconi Anemia
Bone Marrow Diseases
Anemia, Aplastic
Anemia, Hypoplastic, Congenital
Fanconi Anemia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Cockayne Syndrome
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Skin Abnormalities
Xeroderma Pigmentosum
Fetal Diseases
Genetic Diseases, Inborn
alpha 1-Antitrypsin Deficiency
Anemia, Hypoplastic, Congenital
Fanconi Anemia
Dwarfism
Cockayne Syndrome
Eye Diseases, Hereditary
Retinitis Pigmentosa
Heredodegenerative Disorders, Nervous System
Cockayne Syndrome
Metabolism, Inborn Errors
Progeria
Skin Diseases, Genetic
Xeroderma Pigmentosum
Skin and Connective Tissue Diseases
Skin Diseases
Hair Diseases
Photosensitivity Disorders
Xeroderma Pigmentosum
Pigmentation Disorders
Xeroderma Pigmentosum
Skin Abnormalities
Xeroderma Pigmentosum
Skin Diseases, Genetic
Xeroderma Pigmentosum
Nutritional and Metabolic Diseases
Metabolic Diseases
Calcium Metabolism Disorders
Calcinosis
DNA Repair-Deficiency Disorders
Cockayne Syndrome
Fanconi Anemia
Xeroderma Pigmentosum
Metabolism, Inborn Errors
Progeria
Endocrine System Diseases
Dwarfism
Immune System Diseases
Autoimmune Diseases
Autoimmune Diseases of the Nervous System
Demyelinating Autoimmune Diseases, CNS
Diffuse Cerebral Sclerosis of Schilder
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Trisomy
Chromosome Duplication
Trisomy
Disease
Syndrome
Disease Attributes
Diseases in Twins
Emphysema
Subcutaneous Emphysema
alpha 1-Antitrypsin Deficiency
Growth Disorders
Signs and Symptoms
Body Weight
Body Weight Changes
Weight Loss
Emaciation
Cachexia
Neurologic Manifestations
Dyskinesias
Ataxia
Neurobehavioral Manifestations
Intellectual Disability
Reflex, Abnormal
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Hearing Loss, Sensorineural
Vision Disorders
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