MeSH Treeview
Query OMIM entry list
609612
-
FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, WITH SYNERGISTIC DIVERGENCE
→
High-scoring List
Musculoskeletal Diseases
Jaw Diseases
Stomatognathic Diseases
Jaw Diseases
Nervous System Diseases
Central Nervous System Diseases
Ocular Motility Disorders
Cranial Nerve Diseases
Ocular Motility Disorders
Ophthalmoplegia
Neurologic Manifestations
Paralysis
Ophthalmoplegia
Sensation Disorders
Vision Disorders
Diplopia
Eye Diseases
Eye Abnormalities
Eye Diseases, Hereditary
Albinism
Albinism, Oculocutaneous
Eyelid Diseases
Blepharoptosis
Ocular Motility Disorders
Ophthalmoplegia
Vision Disorders
Diplopia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Eye Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Albinism
Albinism, Oculocutaneous
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Albinism, Oculocutaneous
Skin Diseases, Genetic
Albinism
Albinism, Oculocutaneous
Skin and Connective Tissue Diseases
Skin Diseases
Pigmentation Disorders
Hypopigmentation
Albinism
Albinism, Oculocutaneous
Skin Diseases, Genetic
Albinism
Albinism, Oculocutaneous
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Albinism, Oculocutaneous
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease
Syndrome
Fibrosis
Signs and Symptoms
Neurologic Manifestations
Paralysis
Ophthalmoplegia
Sensation Disorders
Vision Disorders
Diplopia
Database Center for Life Science
