당신이 있었기에,우리는 더 많은 답에 가까워질 수 있었습니다.

back to listBack to List

NR1H4

nuclear receptor subfamily 1 group H member 4

HCNC Approved Symbol
NR1H4 (HGNC:7967)
Genomic Coordinates
12:100,473,866 - 100,564,414 (12q23.1)
Synonyms
FXR, RIP14, HRR1, HRR-1
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Cholestasis, progressive familial intrahepatic, 5
617049AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the NR1H4 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results