MeSH Treeview
Query OMIM entry list
606952
OCA1B
ALBINISM, OCULOCUTANEOUS, TYPE IB
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Nervous System Diseases
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Down Syndrome
Eye Diseases
Eye Diseases, Hereditary
Albinism
Albinism, Oculocutaneous
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Down Syndrome
Chromosome Disorders
Down Syndrome
Genetic Diseases, Inborn
Chromosome Disorders
Down Syndrome
Eye Diseases, Hereditary
Albinism
Albinism, Oculocutaneous
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Albinism, Oculocutaneous
Skin Diseases, Genetic
Albinism
Albinism, Oculocutaneous
Skin and Connective Tissue Diseases
Skin Diseases
Pigmentation Disorders
Hypopigmentation
Albinism
Albinism, Oculocutaneous
Skin Diseases, Genetic
Albinism
Albinism, Oculocutaneous
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Albinism, Oculocutaneous
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