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  2. Biological Process

Sphingolipid Metabolic Process

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Diseases Associated With Sphingolipid Metabolic Process

Disease
Parkinsonian Disorders
Liver Cirrhosis, Experimental
Prostatic Neoplasms
Liver Diseases
Ichthyosiform Erythroderma, Brocq Congenital, Nonbullous Form
Ichthyosis, Lamellar
Gaucher Disease
Gaucher Disease, Atypical, Due To Saposin C Deficiency
Gaucher Disease, Perinatal Lethal
Gaucher Disease, Type Iiic
Heart Diseases
Hernia, Diaphragmatic
Hyperkinesis
Pulmonary Hypertension
Intellectual Disability
Krabbe Disease, Atypical, Due To Saposin A Deficiency
Learning Disorders
Leukemia
Leukodystrophy, Globoid Cell
Lewy Body Dementia
Lung Diseases
Lung Neoplasms
Lymphoma, Follicular
Metachromatic Leukodystrophy Due To Saposin B Deficiency
Myelodysplastic Syndromes
Myocardial Ischemia
Nerve Degeneration
Neuroblastoma
Neurotoxicity Syndromes
Parkinson's Disease
Pheochromocytoma
Segawa Syndrome, Autosomal Recessive
Surfactant Metabolism Dysfunction, Pulmonary, 1
Brain Diseases
Tay-Sachs Disease, Ab Variant
Hepatocellular Carcinoma
Catalepsy
Combined Saposin Deficiency
Dyskinesia, Drug-Induced
Limb Dystonia

Related Genes

  • SERINC2
  • SERINC3
  • SERINC5
  • SFTPB
  • SPNS2
  • SPTLC1
  • TH

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