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Query OMIM entry list
601499
RIEG2
RIEGER SYNDROME, TYPE 2
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Stomatognathic Diseases
Stomatognathic System Abnormalities
Tooth Abnormalities
Tooth Diseases
Tooth Abnormalities
Eye Diseases
Eye Abnormalities
Eye Diseases, Hereditary
Ocular Hypertension
Glaucoma
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Eye Abnormalities
Stomatognathic System Abnormalities
Tooth Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Disease
Syndrome
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