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601220	OOCH	OSTEOPOROSIS AND OCULOCUTANEOUS HYPOPIGMENTATION SYNDROME

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Musculoskeletal Diseases

Bone Diseases, Metabolic

Hand Deformities

Nervous System Diseases

Neurologic Manifestations

Sensation Disorders

Vision Disorders

Eye Diseases, Hereditary

Albinism, Oculocutaneous

Vision Disorders

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

Pathological Conditions, Signs and Symptoms

Pathologic Processes

Signs and Symptoms

Neurologic Manifestations

Sensation Disorders

Vision Disorders

Database Center for Life Science