MeSH Treeview
Query OMIM entry list
126070
-
DILUTION, PIGMENTARY
→
High-scoring List
Stomatognathic Diseases
Mouth Diseases
Nervous System Diseases
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Prader-Willi Syndrome
Eye Diseases
Eye Diseases, Hereditary
Albinism
Hemic and Lymphatic Diseases
Hematologic Diseases
Leukocyte Disorders
Phagocyte Bactericidal Dysfunction
Chediak-Higashi Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Prader-Willi Syndrome
Chromosome Disorders
Prader-Willi Syndrome
Genetic Diseases, Inborn
Chromosome Disorders
Prader-Willi Syndrome
Eye Diseases, Hereditary
Albinism
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Skin Diseases, Genetic
Albinism
Skin and Connective Tissue Diseases
Skin Diseases
Pigmentation Disorders
Hypopigmentation
Albinism
Skin Diseases, Genetic
Albinism
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Nutrition Disorders
Overnutrition
Obesity
Prader-Willi Syndrome
Immune System Diseases
Immunologic Deficiency Syndromes
Phagocyte Bactericidal Dysfunction
Chediak-Higashi Syndrome
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Database Center for Life Science
