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Query OMIM entry list
163920
HMGN1
HIGH MOBILITY GROUP NUCLEOSOMAL BINDING PROTEIN 1
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Nervous System Diseases
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Down Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Down Syndrome
Chromosome Disorders
Down Syndrome
Genetic Diseases, Inborn
Chromosome Disorders
Down Syndrome
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Trisomy
Chromosome Duplication
Trisomy
Database Center for Life Science