Disease #01686 (PFIC1 (cholestasis, intrahepatic, familial, progressive, type 1 (PFIC-1)), OMIM:211600)

Official abbreviation PFIC1
Name cholestasis, intrahepatic, familial, progressive, type 1 (PFIC-1)
OMIM ID 211600
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene ATP8B1
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

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00409543 K6850 PubMed: Oishi 2018 - M - Japan - - - - - PFIC1 best corrected visual acuity: 0.7; electroretinogram , rod: severely reduced, cone: mildly reduced CYP4V2 CYP4V2 2 1 LOVD
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