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Ontology Browser

Primary Bile Acid Malabsorption 2 (DOID:9002010)
Annotations: Rat: (2) Mouse: (2) Human: (2) Chinchilla: (2) Bonobo: (2) Dog: (2) Squirrel: (2) Pig: (2)
Parent Terms Term With Siblings Child Terms
Primary Bile Acid Malabsorption 1  
Primary Bile Acid Malabsorption 2  
An autosomal recessive disorder characterized by chronic diarrhea, severe fat-soluble vitamin deficiency, and features of cholestatic liver disease. Caused by homozygous mutation in the SLC51B gene on chromosome 15q22. (OMIM)

Exact Synonyms: PBAM2
Primary IDs: OMIM:619481

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