MeSH Treeview
Query OMIM entry list
607145
DTNBP1
DYSTROBREVIN-BINDING PROTEIN 1
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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
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
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
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