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Query OMIM entry list
600890
HADHA
HYDROXYACYL-CoA DEHYDROGENASE/3-KETOACYL-CoA THIOLASE/ENOYL-CoA HYDRATASE, ALPHA SUBUNIT
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Musculoskeletal Diseases
Muscular Diseases
Mitochondrial Myopathies
Rhabdomyolysis
Myoglobinuria
Digestive System Diseases
Biliary Tract Diseases
Bile Duct Diseases
Cholestasis
Liver Diseases
Fatty Liver
Nervous System Diseases
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Neurologic Manifestations
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Language Development Disorders
Neuromuscular Manifestations
Muscle Hypotonia
Neuromuscular Diseases
Muscular Diseases
Mitochondrial Myopathies
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Eye Diseases
Retinal Diseases
Female Urogenital Diseases and Pregnancy Complications
Pregnancy Complications
Fetal Diseases
Fetal Growth Retardation
Hypertension, Pregnancy-Induced
HELLP Syndrome
Cardiovascular Diseases
Heart Diseases
Cardiomyopathies
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Fetal Diseases
Fetal Growth Retardation
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Nutritional and Metabolic Diseases
Metabolic Diseases
Calcium Metabolism Disorders
Hypocalcemia
Glucose Metabolism Disorders
Hypoglycemia
Lipid Metabolism Disorders
Lipid Metabolism, Inborn Errors
Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Mitochondrial Diseases
Mitochondrial Myopathies
Water-Electrolyte Imbalance
Hypocalcemia
Nutrition Disorders
Malnutrition
Deficiency Diseases
Avitaminosis
Vitamin D Deficiency
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Nondisjunction, Genetic
Uniparental Disomy
Death
Death, Sudden
Sudden Infant Death
Disease
Syndrome
Disease Attributes
Acute Disease
Chronic Disease
Recurrence
Growth Disorders
Fetal Growth Retardation
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Language Development Disorders
Neuromuscular Manifestations
Muscle Hypotonia
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