Disease #02604 (Crigler-Najjar II (Crigler-Najjar syndrome, type II), OMIM:606785)

Official abbreviation Crigler-Najjar II
Name Crigler-Najjar syndrome, type II
OMIM ID 606785
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 8
Phenotype entries for this disease -
Associated with 1 gene UGT1A1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2022-05-30 21:30:48 +02:00 (CEST)


Individuals

8 entries on 1 page. Showing entries 1 - 8.
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00029360 - - - - ? Tunisia Tunisian - - - - Crigler-Najjar II - - - - 1 Giulia Canu
00428749 PatSM PubMed: Ciotti 1998 - - - Italy - - - - - Crigler-Najjar, Crigler-Najjar II see paper UGT1A1 UGT1A1 2 1 Johan den Dunnen
00428750 PatTS PubMed: Ciotti 1999 - - - United States African-American - - - - Crigler-Najjar, Crigler-Najjar II see paper UGT1A1 UGT1A1 2 1 Johan den Dunnen
00428765 patient;Pat12 PubMed: Labrune 2002, PubMed: Petit 2006 - F - Morocco - - - - - Crigler-Najjar, Crigler-Najjar II see paper UGT1A1 UGT1A1 2 1 Johan den Dunnen
00428766 patient PubMed: Chalasani 1997 - M - United States white - - - - Crigler-Najjar, Crigler-Najjar II see paper UGT1A1 UGT1A1 2 1 Johan den Dunnen
00430749 patient PubMed: Minucci 2012 - M - Italy - - - - - Crigler-Najjar, Crigler-Najjar II, favism , see paper; ..., prolonged neonatal jaundice, G6PD deficiency G6PD, UGT1A1 G6PD, UGT1A1 4 1 Johan den Dunnen
00430776 Pat1 PubMed: Huang 2006 - F - India Singapore - - - - Crigler-Najjar, Crigler-Najjar II see paper UGT1A1 UGT1A1 1 1 Johan den Dunnen
00449753 - - - - - - - - - - - Crigler-Najjar II - UGT1A1 UGT1A1 1 1 Zhenkun Li
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