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146390
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CHROMOSOME 18p DELETION SYNDROME
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Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dwarfism
Dwarfism, Pituitary
Dysostoses
Craniofacial Dysostosis
Hypertelorism
Bone Diseases, Endocrine
Dwarfism, Pituitary
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Craniofacial Dysostosis
Hypertelorism
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Hypothalamic Diseases
Pituitary Diseases
Hypopituitarism
Dwarfism, Pituitary
Neurologic Manifestations
Neurobehavioral Manifestations
Communication Disorders
Learning Disorders
Intellectual Disability
Eye Diseases
Eye Abnormalities
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Abnormalities, Severe Teratoid
Chromosome Disorders
Eye Abnormalities
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Craniofacial Dysostosis
Hypertelorism
Genetic Diseases, Inborn
Chromosome Disorders
Skin and Connective Tissue Diseases
Skin Diseases
Hair Diseases
Hypotrichosis
Alopecia
Endocrine System Diseases
Dwarfism
Dwarfism, Pituitary
Pituitary Diseases
Hypopituitarism
Dwarfism, Pituitary
Immune System Diseases
Immunologic Deficiency Syndromes
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Alopecia
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Translocation, Genetic
Disease
Syndrome
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Communication Disorders
Learning Disorders
Intellectual Disability
Database Center for Life Science
