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Query OMIM entry list
203200
OCA2
ALBINISM, OCULOCUTANEOUS, TYPE II
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Neoplasms
Neoplasms by Histologic Type
Neoplasms, Glandular and Epithelial
Carcinoma
Carcinoma, Basal Cell
Carcinoma, Squamous Cell
Neoplasms, Basal Cell
Carcinoma, Basal Cell
Neoplasms, Squamous Cell
Carcinoma, Squamous Cell
Neoplasms by Site
Skin Neoplasms
Musculoskeletal Diseases
Bone Diseases
Muscular Diseases
Digestive System Diseases
Gastrointestinal Diseases
Respiratory Tract Diseases
Nervous System Diseases
Cranial Nerve Diseases
Ocular Motility Disorders
Nystagmus, Pathologic
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Prader-Willi Syndrome
Neuromuscular Diseases
Muscular Diseases
Eye Diseases
Eye Diseases, Hereditary
Albinism
Albinism, Ocular
Albinism, Oculocutaneous
Hermanski-Pudlak Syndrome
Ocular Motility Disorders
Nystagmus, Pathologic
Male Urogenital Diseases
Urologic Diseases
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Cardiovascular Diseases
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
Congenital Abnormalities
Abnormalities, Multiple
Prader-Willi Syndrome
Chromosome Disorders
Prader-Willi Syndrome
Genetic Diseases, Inborn
Blood Coagulation Disorders, Inherited
Hermanski-Pudlak Syndrome
Chromosome Disorders
Prader-Willi Syndrome
Eye Diseases, Hereditary
Albinism
Albinism, Ocular
Albinism, Oculocutaneous
Hermanski-Pudlak Syndrome
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Albinism, Ocular
Albinism, Oculocutaneous
Hermanski-Pudlak Syndrome
Skin Diseases, Genetic
Albinism
Albinism, Ocular
Albinism, Oculocutaneous
Hermanski-Pudlak Syndrome
Skin and Connective Tissue Diseases
Skin Diseases
Pigmentation Disorders
Hyperpigmentation
Melanosis
Hypopigmentation
Albinism
Albinism, Ocular
Albinism, Oculocutaneous
Hermanski-Pudlak Syndrome
Skin Diseases, Genetic
Albinism
Albinism, Ocular
Albinism, Oculocutaneous
Hermanski-Pudlak Syndrome
Skin Neoplasms
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Albinism, Ocular
Albinism, Oculocutaneous
Hermanski-Pudlak Syndrome
Nutrition Disorders
Overnutrition
Obesity
Prader-Willi Syndrome
Endocrine System Diseases
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Translocation, Genetic
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