Disease #00310 (favism (favism, susceptibility to), OMIM:134700)

Official abbreviation favism
Name favism, susceptibility to
OMIM ID 134700
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 12
Phenotype entries for this disease 8
Associated with 1 gene G6PD
Associated tissues -
Disease features -
Remarks X-linked dominant; merged with OMIM 305900
Date created 2014-01-24 11:35:49 +01:00 (CET)
Date last edited 2019-08-05 19:51:00 +02:00 (CEST)


Individuals

12 entries on 1 page. Showing entries 1 - 12.
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00004487 - - - F ? Italy - - - - - favism favism4 G6PD G6PD 1 1 Ettore Capoluongo
00228933 Fam43 PubMed: Pissard 2006 - - - France - - - - - favism, pyr.kin. deficiency - PKLR PKLR 1 1 Richard van Wijk
00228934 Fam44 PubMed: Pissard 2006 - - - France - - - - - favism, PVNH7 - PKLR PKLR 1 1 Richard van Wijk
00228937 Fam47 PubMed: Pissard 2006 - - - France - - - - - favism, pyr.kin. deficiency - PKLR PKLR 1 1 Richard van Wijk
00300282 NBS_83162 - - M - China Chinese - - - - favism enzyme activity of G6PD: 1.3 IU/gHb (reference:>2 IU/gHb) G6PD G6PD 1 1 Wenjuan Qiu
00300283 NBS_83841 - - M - China Chinese - - - - favism enzyme activity of G6PD: 1.0 IU/gHb (reference:>2 IU/gHb) G6PD G6PD 1 1 Wenjuan Qiu
00300284 NBS_83847 - - M ? China Chinese - - - - favism enzyme activity of G6PD: 1.4 IU/gHb (reference:>2 IU/gHb) G6PD G6PD 1 1 Wenjuan Qiu
00300285 NBS_84010 - - M ? China Chinese - - - - favism enzyme activity of G6PD: 1.5 IU/gHb (reference:>2 IU/gHb) G6PD G6PD 1 1 Wenjuan Qiu
00403160 FamIPatI1 PubMed: Jaouani 2017 2-generation family, 1 affected M - Tunisia - - - - - favism, pyr.kin. deficiency hemolytic anemia triggered by fava beans ingestion G6PD, PKLR G6PD, PKLR 2 1 Johan den Dunnen
00430524 Pat11 PubMed: D'Apolito 2007 - M - Italy - - - - - Crigler-Najjar, favism see paper; ..., increased bilirubin production due to hemolysis, glucose-6-phosphate dehydrogenase G6PD, UGT1A1 G6PD, 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
00435026 G6PD-863 PubMed: Alcántara-Ortigoza 2022 - M no Mexico Mestizo >01y06m - yes - favism G6PD deficiency in a male identified through newborn screening (G6PD-1125). Also, the same variant was identified in his heterozygous mother, and in another unrelated hemizygous male (G6PD-780) also carrying G6PD deficiency identified by newborn screening. G6PD G6PD 1 2 Miguel Angel Alcántara-Ortigoza
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