MeSH Treeview
Query gene list
392561
OR3B1P
olfactory receptor, family 3, subfamily B, member 1 pseudogene
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High-scoring List
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Incontinentia Pigmenti
Skin Abnormalities
Incontinentia Pigmenti
Genetic Diseases, Inborn
Skin Diseases, Genetic
Incontinentia Pigmenti
Skin and Connective Tissue Diseases
Skin Diseases
Pigmentation Disorders
Incontinentia Pigmenti
Skin Abnormalities
Incontinentia Pigmenti
Skin Diseases, Genetic
Incontinentia Pigmenti
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Chromosome Inversion
Database Center for Life Science
