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Familial Methionine Malabsorption: Disease Bioinformatics

Research of Familial Methionine Malabsorption has been linked to Malabsorption Syndrome, Diarrhea, Pseudohypoparathyroidism, Homocystinuria, Congenital Glucose-galactose Malabsorption. The study of Familial Methionine Malabsorption has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Familial Methionine Malabsorption include Transport, Water Transport, Amino Acid Transport. These pathways help researchers understand Familial Methionine Malabsorption in relation to NEPHROGENIC DIABETES INSIPIDUS.

Familial Methionine Malabsorption Bioinformatics Tool

Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Familial Methionine Malabsorption below! For more information on how to use Laverne, please read the How to Guide.
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Related Genes

Familial Methionine Malabsorption has been researched against:

Related Pathways

Familial Methionine Malabsorption has been linked to:

Alternate Names

Familial Methionine Malabsorption is also known as Methionine Malabsorption Syndrome.