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235730
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MOWAT-WILSON SYNDROME
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Musculoskeletal Diseases
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Digestive System Diseases
Digestive System Abnormalities
Hirschsprung Disease
Gastrointestinal Diseases
Intestinal Diseases
Colonic Diseases
Megacolon
Hirschsprung Disease
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Epilepsy
Seizures
Spinal Cord Diseases
Muscular Atrophy, Spinal
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Neural Tube Defects
Neurodegenerative Diseases
Motor Neuron Disease
Muscular Atrophy, Spinal
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Seizures
Neuromuscular Diseases
Motor Neuron Disease
Muscular Atrophy, Spinal
Muscular Atrophy, Spinal
Eye Diseases
Eye Abnormalities
Coloboma
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
Heart Diseases
Heart Defects, Congenital
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Cardiovascular Abnormalities
Heart Defects, Congenital
Digestive System Abnormalities
Hirschsprung Disease
Eye Abnormalities
Coloboma
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Neural Tube Defects
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Chromosome Breakage
Translocation, Genetic
Disease
Syndrome
Disease Attributes
Facies
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Seizures
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