Disease #02395 (PFIC2 (cholestasis, intrahepatic, familial, progressive, type 2 (PFIC-2)), OMIM:601847)

Official abbreviation PFIC2
Name cholestasis, intrahepatic, familial, progressive, type 2 (PFIC-2)
OMIM ID 601847
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 7
Phenotype entries for this disease -
Associated with 1 gene ABCB11
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

7 entries on 1 page. Showing entries 1 - 7.
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00464318 - - - F yes Egypt - - - - - PFIC2 - - ABCB11 1 1 Mohamed A. Elmonem
00464319 - - - M yes Egypt - - - - - PFIC2 - - ABCB11 1 1 Mohamed A. Elmonem
00464320 - - - F yes Egypt - - - - - PFIC2 - - ABCB11 1 1 Mohamed A. Elmonem
00464321 - - - M yes Egypt - - - - - PFIC2 - - ABCB11 1 1 Mohamed A. Elmonem
00464322 - - - M yes Egypt - - - - - PFIC2 - - ABCB11 1 1 Mohamed A. Elmonem
00464323 - - - F yes Egypt - - - - - PFIC2 - - ABCB11 1 1 Mohamed A. Elmonem
00464324 - - - F yes Egypt - - - - - PFIC2 - - ABCB11 1 1 Mohamed A. Elmonem
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