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Query OMIM entry list
603867
PEX11B
PEROXISOME BIOGENESIS FACTOR 11B
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Digestive System Diseases
Liver Diseases
Zellweger Syndrome
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Peroxisomal Disorders
Zellweger Syndrome
Neurologic Manifestations
Neuromuscular Manifestations
Muscle Hypotonia
Male Urogenital Diseases
Urologic Diseases
Kidney Diseases
Zellweger Syndrome
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Zellweger Syndrome
Pregnancy Complications
Fetal Diseases
Fetal Growth Retardation
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Zellweger Syndrome
Fetal Diseases
Fetal Growth Retardation
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Peroxisomal Disorders
Zellweger Syndrome
Peroxisomal Disorders
Zellweger Syndrome
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Peroxisomal Disorders
Zellweger Syndrome
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Peroxisomal Disorders
Zellweger Syndrome
Peroxisomal Disorders
Zellweger Syndrome
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Growth Disorders
Fetal Growth Retardation
Signs and Symptoms
Neurologic Manifestations
Neuromuscular Manifestations
Muscle Hypotonia
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