Disease #02487 (ASGD5 (dysgenesis, anterior segment, type 5, multiple subtypes), OMIM:604229)

Official abbreviation ASGD5
Name dysgenesis, anterior segment, type 5, multiple subtypes
OMIM ID 604229
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 3 genes CYP1B1, PAX6, PITX2
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

5 entries on 1 page. Showing entries 1 - 5.
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00051908 - - - - ? - - - - - - ASGD5 Peters' anomaly CYP1B1 CYP1B1 1 1 Johan den Dunnen
00051909 - - - - ? - - - - - - ASGD5 Peters' anomaly CYP1B1 CYP1B1 1 1 Johan den Dunnen
00051948 - - - - ? - - - - - - ASGD5 Peters' anomaly CYP1B1 CYP1B1 1 1 Johan den Dunnen
00054893 - - - - - - white - - - - ASGD5 Peters anomaly, congenital glaucoma; syndromic CYP1B1 CYP1B1 1 1 Elena Semina
00054894 - - - - - - - - - - - ASGD5 Peters anomaly, congenital glaucoma; Syndromic CYP1B1 CYP1B1 5 1 Elena Semina
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