MeSH Treeview
Query OMIM entry list
203100
OCA1A
ALBINISM, OCULOCUTANEOUS, TYPE IA
→
High-scoring List
Neoplasms
Neoplasms by Histologic Type
Neoplasms, Germ Cell and Embryonal
Neuroectodermal Tumors
Neuroendocrine Tumors
Melanoma
Melanoma, Experimental
Neoplasms, Nerve Tissue
Neuroectodermal Tumors
Neuroendocrine Tumors
Melanoma
Melanoma, Experimental
Nevi and Melanomas
Melanoma
Melanoma, Experimental
Neoplasms, Experimental
Melanoma, Experimental
Musculoskeletal Diseases
Jaw Diseases
Jaw Abnormalities
Cleft Palate
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Holoprosencephaly
Maxillofacial Abnormalities
Jaw Abnormalities
Cleft Palate
Stomatognathic Diseases
Jaw Diseases
Jaw Abnormalities
Cleft Palate
Mouth Diseases
Lip Diseases
Cleft Lip
Mouth Abnormalities
Cleft Lip
Cleft Palate
Stomatognathic System Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Cleft Palate
Mouth Abnormalities
Cleft Lip
Cleft Palate
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Deafness
Nervous System Diseases
Cranial Nerve Diseases
Ocular Motility Disorders
Nystagmus, Pathologic
Nystagmus, Congenital
Nervous System Malformations
Agenesis of Corpus Callosum
Holoprosencephaly
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Down Syndrome
Prader-Willi Syndrome
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Vision Disorders
Blindness
Eye Diseases
Eye Abnormalities
Eye Diseases, Hereditary
Albinism
Albinism, Ocular
Albinism, Oculocutaneous
Hermanski-Pudlak Syndrome
Lens Diseases
Cataract
Ocular Motility Disorders
Nystagmus, Pathologic
Nystagmus, Congenital
Retinal Diseases
Vision Disorders
Blindness
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Hemolytic
Anemia, Hemolytic, Congenital
Anemia, Sickle Cell
Thalassemia
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
Hemoglobinopathies
Anemia, Sickle Cell
Thalassemia
Hemorrhagic Disorders
Platelet Storage Pool Deficiency
Hermanski-Pudlak Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Down Syndrome
Holoprosencephaly
Prader-Willi Syndrome
Waardenburg Syndrome
Chromosome Disorders
Down Syndrome
Holoprosencephaly
Prader-Willi Syndrome
Eye Abnormalities
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Holoprosencephaly
Maxillofacial Abnormalities
Jaw Abnormalities
Cleft Palate
Nervous System Malformations
Agenesis of Corpus Callosum
Holoprosencephaly
Holoprosencephaly
Skin Abnormalities
Epidermolysis Bullosa
Stomatognathic System Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Cleft Palate
Mouth Abnormalities
Cleft Lip
Cleft Palate
Genetic Diseases, Inborn
Anemia, Hemolytic, Congenital
Anemia, Sickle Cell
Thalassemia
Blood Coagulation Disorders, Inherited
Hermanski-Pudlak Syndrome
Chromosome Disorders
Down Syndrome
Holoprosencephaly
Prader-Willi Syndrome
Eye Diseases, Hereditary
Albinism
Albinism, Ocular
Albinism, Oculocutaneous
Hermanski-Pudlak Syndrome
Hemoglobinopathies
Anemia, Sickle Cell
Thalassemia
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
Epidermolysis Bullosa
Infant, Newborn, Diseases
Nystagmus, Congenital
Skin and Connective Tissue Diseases
Skin Diseases
Pigmentation Disorders
Hypopigmentation
Albinism
Albinism, Ocular
Albinism, Oculocutaneous
Hermanski-Pudlak Syndrome
Skin Abnormalities
Epidermolysis Bullosa
Skin Diseases, Genetic
Albinism
Albinism, Ocular
Albinism, Oculocutaneous
Hermanski-Pudlak Syndrome
Epidermolysis Bullosa
Skin Diseases, Vesiculobullous
Epidermolysis Bullosa
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
Animal Diseases
Cat Diseases
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Disease
Syndrome
Signs and Symptoms
Neurologic Manifestations
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Vision Disorders
Blindness
Database Center for Life Science
