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151800	-	LIPOMATOSIS, FAMILIAL BENIGN CERVICAL

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Musculoskeletal Diseases

Bone Diseases, Developmental

Congenital Hypothyroidism

Bone Diseases, Endocrine

Congenital Hypothyroidism

Muscular Diseases

Rheumatic Diseases

Nervous System Diseases

Autonomic Nervous System Diseases

Neuromuscular Diseases

Muscular Diseases

Peripheral Nervous System Diseases

Retinal Neoplasms

Retinal Diseases

Retinal Neoplasms

Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Congenital Abnormalities

Chromosome Disorders

Genetic Diseases, Inborn

Chromosome Disorders

Congenital Hypothyroidism

Metabolism, Inborn Errors

Purine-Pyrimidine Metabolism, Inborn Errors

Skin and Connective Tissue Diseases

Lipomatosis, Multiple Symmetrical

Nutritional and Metabolic Diseases

Metabolic Diseases

Lipid Metabolism Disorders

Hyperlipidemias

Hyperlipoproteinemias

Lipomatosis, Multiple Symmetrical

Metabolism, Inborn Errors

Purine-Pyrimidine Metabolism, Inborn Errors

Endocrine System Diseases

Congenital Hypothyroidism

Thyroid Diseases

Congenital Hypothyroidism

Pathological Conditions, Signs and Symptoms

Pathological Conditions, Anatomical

Pathologic Processes

Chromosome Aberrations

Chromosome Deletion

Disease Attributes

Disease Susceptibility

Genetic Predisposition to Disease

Database Center for Life Science