Disease #00090 (Neonatal Hyperbilirubinemia, OMIM:237900)

Official abbreviation -
Name Neonatal Hyperbilirubinemia
OMIM ID 237900
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 7
Phenotype entries for this disease -
Associated with 2 genes SLCO1B1, UGT1A1
Associated tissues -
Disease features -
Remarks -


Individuals

7 entries on 1 page. Showing entries 1 - 7.
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00000529 Fei-Liang Wong et al.(2009) - Malaysia Chinese - - - Neonatal Hyperbilirubinemia - SLCO1B1 SLCO1B1 4 1 Nur Aisyah Athirah
00000530 Fei Liang Wong et al.(2012) - Malaysia Malay - Patients are neonates born from January 2007 till June 2007 - Neonatal Hyperbilirubinemia - SLCO1B1 SLCO1B1 5 1 Nur Aisyah Athirah
00000531 Fei Liang Wong et al.(2012) - Malaysia Chinese - Patients are neonates born from January 2007 till June 2007 - Neonatal Hyperbilirubinemia - SLCO1B1 SLCO1B1 5 1 Nur Aisyah Athirah
00000532 Fei Liang Wong et al.(2012) - Malaysia Indian - Patients are neonates born from January 2007 till June 2007 - Neonatal Hyperbilirubinemia - SLCO1B1 SLCO1B1 5 1 Nur Aisyah Athirah
00000581 Feiliang Wong et al.(2013) - (Seremban, Negeri Sembilan) - - - - Neonatal Hyperbilirubinemia - G6PD, SLCO1B1, UGT1A1 G6PD, SLCO1B1, UGT1A1 11 1 Nur Aisyah Athirah
00000593 S Shwe et al.(2020) - Malaysia - - - - Neonatal Hyperbilirubinemia - HBA2 HBA2 2 1 Nur Aisyah Athirah
00000596 Schwe Sin et al.(2020): http://iosrjournals.org/iosr-jdms/papers/Vol19-issue5/Series-1/J1905014449.pdf - Malaysia Indian - - - Neonatal Hyperbilirubinemia - UGT1A1 UGT1A1 1 1 Nur Aisyah Athirah
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