Disease #01688 (CANDF2 (candidiasis, familial, type 2 (CANDF-2)), OMIM:212050)

Official abbreviation CANDF2
Name candidiasis, familial, type 2 (CANDF-2)
OMIM ID 212050
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 CARD9
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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00409545 K6169 PubMed: Oishi 2018 - M - Japan - - - - - CANDF2 best corrected visual acuity: 0.04; electroretinogram , rod: non- recordable, cone: severely reduced CYP4V2 CYP4V2 2 1 LOVD
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