MeSH Treeview
Query OMIM entry list
203290
OCA3
ALBINISM, OCULOCUTANEOUS, TYPE III
→
High-scoring List
Neoplasms
Neoplasms by Histologic Type
Neoplasms, Glandular and Epithelial
Carcinoma
Carcinoma, Squamous Cell
Neoplasms, Squamous Cell
Carcinoma, Squamous Cell
Neoplasms by Site
Skin Neoplasms
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
Congenital Abnormalities
Chromosome Disorders
Genetic Diseases, Inborn
Blood Coagulation Disorders, Inherited
Hermanski-Pudlak Syndrome
Chromosome Disorders
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
Erythema
Keratosis
Pigmentation Disorders
Hyperpigmentation
Melanosis
Lentigo
Hypopigmentation
Albinism
Albinism, Oculocutaneous
Hermanski-Pudlak Syndrome
Skin Diseases, Genetic
Albinism
Albinism, Oculocutaneous
Hermanski-Pudlak Syndrome
Skin Neoplasms
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
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Disease Attributes
Diseases in Twins
Database Center for Life Science
