Gendoo - MeSH tree view

MeSH Treeview

Query OMIM entry list

191270	TYRL	TYROSINASE-LIKE

→ High-scoring List

Eye Diseases, Hereditary

Albinism, Oculocutaneous

Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Genetic Diseases, Inborn

Eye Diseases, Hereditary

Albinism, Oculocutaneous

Metabolism, Inborn Errors

Amino Acid Metabolism, Inborn Errors

Albinism, Oculocutaneous

Skin Diseases, Genetic

Albinism, Oculocutaneous

Skin and Connective Tissue Diseases

Pigmentation Disorders

Hypopigmentation

Albinism, Oculocutaneous

Skin Diseases, Genetic

Albinism, Oculocutaneous

Nutritional and Metabolic Diseases

Metabolic Diseases

Metabolism, Inborn Errors

Amino Acid Metabolism, Inborn Errors

Albinism, Oculocutaneous

Database Center for Life Science