Hypercholanemia, familial, 2
MONDO:0031003Also known as: FHCA2, NTCP Deficiency, hypercholanemia, familial 2
1 clinical trial for this condition and its sub-types.
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Disease
(680)
Metabolic disease
(233)
Inherited lipid metabolism disorder
(189)
Hereditary disease
(176)
Inborn errors of metabolism
(45)
Human disease
(14)
Disease of genetic or genomic mechanism
(2)
Inborn disorder of bile acid synthesis
(2)
Steroid metabolism disease
(1)
Disease by developmental or physiological process
(0)