MeSH Treeview
Query OMIM entry list
600857
SDHA
SUCCINATE DEHYDROGENASE COMPLEX, SUBUNIT A, FLAVOPROTEIN
→
High-scoring List
Neoplasms
Precancerous Conditions
Xeroderma Pigmentosum
Musculoskeletal Diseases
Muscular Diseases
Mitochondrial Myopathies
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Leigh Disease
Cranial Nerve Diseases
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Optic Atrophy, Autosomal Dominant
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Optic Atrophies, Hereditary
Optic Atrophy, Autosomal Dominant
Neuromuscular Diseases
Muscular Diseases
Mitochondrial Myopathies
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Eye Diseases
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Optic Atrophy, Autosomal Dominant
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Optic Atrophy, Autosomal Dominant
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Skin Abnormalities
Xeroderma Pigmentosum
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Optic Atrophy, Autosomal Dominant
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Optic Atrophies, Hereditary
Optic Atrophy, Autosomal Dominant
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Leigh Disease
Carbohydrate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors
Leigh Disease
Skin Diseases, Genetic
Xeroderma Pigmentosum
Skin and Connective Tissue Diseases
Skin Diseases
Photosensitivity Disorders
Xeroderma Pigmentosum
Pigmentation Disorders
Xeroderma Pigmentosum
Skin Abnormalities
Xeroderma Pigmentosum
Skin Diseases, Genetic
Xeroderma Pigmentosum
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Leigh Disease
DNA Repair-Deficiency Disorders
Xeroderma Pigmentosum
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Leigh Disease
Carbohydrate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors
Leigh Disease
Mitochondrial Diseases
Leigh Disease
Mitochondrial Myopathies
Optic Atrophy, Autosomal Dominant
Database Center for Life Science
