MeSH Treeview
Query OMIM entry list
300500
OA1
ALBINISM, OCULAR, TYPE I
→
High-scoring List
Neoplasms
Neoplasms by Histologic Type
Neoplasms, Germ Cell and Embryonal
Neuroectodermal Tumors
Neuroendocrine Tumors
Melanoma
Neoplasms, Nerve Tissue
Neuroectodermal Tumors
Neuroendocrine Tumors
Melanoma
Nevi and Melanomas
Melanoma
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dwarfism
Osteochondrodysplasias
Chondrodysplasia Punctata
Muscular Diseases
Muscle Weakness
Paralyses, Familial Periodic
Nervous System Diseases
Cranial Nerve Diseases
Ocular Motility Disorders
Nystagmus, Pathologic
Nystagmus, Congenital
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Neuromuscular Manifestations
Muscle Weakness
Sensation Disorders
Vision Disorders
Color Vision Defects
Neuromuscular Diseases
Muscular Diseases
Paralyses, Familial Periodic
Neuromuscular Junction Diseases
Myasthenic Syndromes, Congenital
Eye Diseases
Eye Abnormalities
Eye Diseases, Hereditary
Albinism
Albinism, Ocular
Albinism, Oculocutaneous
Ocular Motility Disorders
Nystagmus, Pathologic
Nystagmus, Congenital
Retinal Diseases
Vision Disorders
Color Vision Defects
Male Urogenital Diseases
Urogenital Abnormalities
Disorders of Sex Development
46, XY Disorders of Sex Development
Kallmann Syndrome
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urogenital Abnormalities
Disorders of Sex Development
46, XY Disorders of Sex Development
Kallmann Syndrome
Cardiovascular Diseases
Vascular Diseases
Embolism and Thrombosis
Thrombosis
Venous Thrombosis
Thrombophlebitis
Peripheral Vascular Diseases
Phlebitis
Thrombophlebitis
Vasculitis
Phlebitis
Thrombophlebitis
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Eye Abnormalities
Skin Abnormalities
Ichthyosis
Ichthyosis, X-Linked
Urogenital Abnormalities
Disorders of Sex Development
46, XY Disorders of Sex Development
Kallmann Syndrome
Genetic Diseases, Inborn
Dwarfism
Eye Diseases, Hereditary
Albinism
Albinism, Ocular
Albinism, Oculocutaneous
Genetic Diseases, X-Linked
Ichthyosis, X-Linked
Kallmann Syndrome
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Albinism, Ocular
Albinism, Oculocutaneous
Metal Metabolism, Inborn Errors
Paralyses, Familial Periodic
Steroid Metabolism, Inborn Errors
Ichthyosis, X-Linked
Myasthenic Syndromes, Congenital
Skin Diseases, Genetic
Albinism
Albinism, Ocular
Albinism, Oculocutaneous
Ichthyosis, X-Linked
Infant, Newborn, Diseases
Ichthyosis
Ichthyosis, X-Linked
Nystagmus, Congenital
Skin and Connective Tissue Diseases
Skin Diseases
Keratosis
Ichthyosis
Ichthyosis, X-Linked
Pigmentation Disorders
Hypopigmentation
Albinism
Albinism, Ocular
Albinism, Oculocutaneous
Skin Abnormalities
Ichthyosis
Ichthyosis, X-Linked
Skin Diseases, Genetic
Albinism
Albinism, Ocular
Albinism, Oculocutaneous
Ichthyosis, X-Linked
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Albinism, Ocular
Albinism, Oculocutaneous
Metal Metabolism, Inborn Errors
Paralyses, Familial Periodic
Steroid Metabolism, Inborn Errors
Ichthyosis, X-Linked
Endocrine System Diseases
Dwarfism
Gonadal Disorders
Disorders of Sex Development
46, XY Disorders of Sex Development
Kallmann Syndrome
Hypogonadism
Kallmann Syndrome
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Sex Chromosome Aberrations
Disease
Syndrome
Disease Attributes
Chronic Disease
Muscle Weakness
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Neuromuscular Manifestations
Muscle Weakness
Sensation Disorders
Vision Disorders
Color Vision Defects
Database Center for Life Science
