Disease #01180 (ASGD1 (dysgenesis, anterior segment, type 1 (ASGD1)), OMIM:107250)

Official abbreviation ASGD1
Name dysgenesis, anterior segment, type 1 (ASGD1)
OMIM ID 107250
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 2 genes FOXE3, PITX3
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

2 entries on 1 page. Showing entries 1 - 2.
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00382116 81 PubMed: Patel 2019 - ? - United Kingdom (Great Britain) - - - - - ASGD1 anterior segment developmental anomalies including glaucoma; MIM, 107250 FOXE3 FOXE3 1 1 LOVD
00411261 198801 - - F yes Saudi Arabia - - - - - ASGD1 Visual impairment, Abnormal eye morphology, Congenital primary aphakia FOXE3 FOXE3 1 1 Andreas Laner
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