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606526
MLPH
MELANOPHILIN
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Eye Diseases
Eye Diseases, Hereditary
Albinism
Albinism, Oculocutaneous
Hermanski-Pudlak Syndrome
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Coagulation Disorders
Blood Coagulation Disorders, Inherited
Hermanski-Pudlak Syndrome
Platelet Storage Pool Deficiency
Hermanski-Pudlak Syndrome
Blood Platelet Disorders
Platelet Storage Pool Deficiency
Hermanski-Pudlak Syndrome
Hemorrhagic Disorders
Platelet Storage Pool Deficiency
Hermanski-Pudlak Syndrome
Leukocyte Disorders
Phagocyte Bactericidal Dysfunction
Chediak-Higashi Syndrome
Lymphatic Diseases
Histiocytosis
Histiocytosis, Non-Langerhans-Cell
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Blood Coagulation Disorders, Inherited
Hermanski-Pudlak Syndrome
Eye Diseases, Hereditary
Albinism
Albinism, Oculocutaneous
Hermanski-Pudlak Syndrome
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Albinism, Oculocutaneous
Hermanski-Pudlak Syndrome
Skin Diseases, Genetic
Albinism
Albinism, Oculocutaneous
Hermanski-Pudlak Syndrome
Skin and Connective Tissue Diseases
Skin Diseases
Pigmentation Disorders
Hypopigmentation
Albinism
Albinism, Oculocutaneous
Hermanski-Pudlak Syndrome
Skin Diseases, Genetic
Albinism
Albinism, Oculocutaneous
Hermanski-Pudlak Syndrome
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Albinism, Oculocutaneous
Hermanski-Pudlak Syndrome
Immune System Diseases
Immunologic Deficiency Syndromes
Phagocyte Bactericidal Dysfunction
Chediak-Higashi Syndrome
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease
Syndrome
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