Disease #02331 (GLC3B (glaucoma, congenital, primary infantile, type 3B (GLC-3B)), OMIM:600975)

Official abbreviation GLC3B
Name glaucoma, congenital, primary infantile, type 3B (GLC-3B)
OMIM ID 600975
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 2 genes CYP1B1, LTBP2
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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00384346 13819 PubMed: Wang 2019 - F - China - - - - - GLC3B - CYP1B1 CYP1B1 2 1 LOVD
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