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607872
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MONOSOMY 1p36 SYNDROME
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Musculoskeletal Diseases
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Epilepsy
Seizures
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Psychomotor Disorders
Seizures
Sensation Disorders
Hearing Disorders
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Chromosome Disorders
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Genetic Diseases, Inborn
Chromosome Disorders
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Chromosome Breakage
Disease
Syndrome
Disease Attributes
Facies
Growth Disorders
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Psychomotor Disorders
Seizures
Sensation Disorders
Hearing Disorders
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