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Query OMIM entry list
601757
PEX7
PEROXISOME BIOGENESIS FACTOR 7
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Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Osteochondrodysplasias
Chondrodysplasia Punctata
Chondrodysplasia Punctata, Rhizomelic
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Peroxisomal Disorders
Refsum Disease
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Refsum Disease
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Refsum Disease
Neuromuscular Diseases
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Refsum Disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Refsum Disease
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Refsum Disease
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Peroxisomal Disorders
Refsum Disease
Peroxisomal Disorders
Chondrodysplasia Punctata, Rhizomelic
Refsum Disease
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Peroxisomal Disorders
Refsum Disease
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Peroxisomal Disorders
Refsum Disease
Peroxisomal Disorders
Chondrodysplasia Punctata, Rhizomelic
Refsum Disease
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Chromosome Inversion
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