MeSH Treeview
Query OMIM entry list
258870
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ORNITHINE AMINOTRANSFERASE DEFICIENCY
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Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Marfan Syndrome
Nervous System Diseases
Neurologic Manifestations
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Intellectual Disability
Neuromuscular Manifestations
Muscular Atrophy
Sensation Disorders
Vision Disorders
Blindness
Eye Diseases
Eye Diseases, Hereditary
Gyrate Atrophy
Retinal Diseases
Retinal Degeneration
Retinal Detachment
Uveal Diseases
Choroid Diseases
Gyrate Atrophy
Vision Disorders
Blindness
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
Marfan Syndrome
Heart Diseases
Heart Defects, Congenital
Marfan Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Marfan Syndrome
Cardiovascular Abnormalities
Heart Defects, Congenital
Marfan Syndrome
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Gyrate Atrophy
Marfan Syndrome
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Marfan Syndrome
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Muscular Atrophy
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Disease
Syndrome
Disease Attributes
Disease Progression
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Intellectual Disability
Neuromuscular Manifestations
Muscular Atrophy
Sensation Disorders
Vision Disorders
Blindness
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