Disease #00878 (Crigler-Najjar I (Crigler-Najjar syndrome, type I), OMIM:218800)

Official abbreviation Crigler-Najjar I
Name Crigler-Najjar syndrome, type I
OMIM ID 218800
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 8
Phenotype entries for this disease 1
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 21:30:33 +02:00 (CEST)


Individuals

8 entries on 1 page. Showing entries 1 - 8.
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00306850 P19 PubMed: Trabelsi 2021, Journal: Trabelsi 2021 - M - Tunisia - - - - - Crigler-Najjar I severe unconjugated hyperbilirubinemia, nuclear kernicterus UGT1A1 UGT1A1 2 1 Nawel Trabelsi
00428744 PatBG PubMed: Ciotti 1997 - - - El Salvador - - - - - Crigler-Najjar, Crigler-Najjar I see paper UGT1A1 UGT1A1 1 1 Johan den Dunnen
00428745 PatGD PubMed: Ciotti 1997 - - - United States African-American - - - - Crigler-Najjar, Crigler-Najjar I see paper UGT1A1 UGT1A1 2 1 Johan den Dunnen
00428746 PatYA PubMed: Ciotti 1997 - M - Turkey - - - - - Crigler-Najjar, Crigler-Najjar I see paper UGT1A1 UGT1A1 1 1 Johan den Dunnen
00428747 PatSS PubMed: Ciotti 1995 - - - United States - - - - - Crigler-Najjar, Crigler-Najjar I see paper UGT1A1 UGT1A1 1 1 Johan den Dunnen
00428748 PatCF PubMed: Ciotti 1998 - F - Italy - - - - - Crigler-Najjar, Crigler-Najjar I see paper UGT1A1 UGT1A1 2 1 Johan den Dunnen
00428799 patient PubMed: Sappal 2002 2-generation family, 1 affected, unaffected heterozygous carrier parents - - United States - - - - - Crigler-Najjar, Crigler-Najjar I see paper UGT1A1 UGT1A1 3 1 Johan den Dunnen
00430892 patient PubMed: Canu 2013 - - - - - - - - - Crigler-Najjar, Crigler-Najjar I - UGT1A1 UGT1A1 1 1 Johan den Dunnen
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