Disease #02487

Official abbreviation Peters
Name Peters anomaly
OMIM ID 604229
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 3 genes CYP1B1, PAX6, PITX2
Associated tissues -
Disease features -
Remarks -


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00051908 - - - - ? - - - 0 - - Peters Peters' anomaly CYP1B1 CYP1B1 1 1 Johan den Dunnen
00051909 - - - - ? - - - 0 - - Peters Peters' anomaly CYP1B1 CYP1B1 1 1 Johan den Dunnen
00051948 - - - - ? - - - 0 - - Peters Peters' anomaly CYP1B1 CYP1B1 1 1 Johan den Dunnen
00054893 - - - - - - Caucasian - 0 - - Peters Peters anomaly, congenital glaucoma; syndromic CYP1B1 CYP1B1 1 1 Elena Semina
00054894 - - - - - - - - 0 - - Peters Peters anomaly, congenital glaucoma; Syndromic CYP1B1 CYP1B1 5 1 Elena Semina
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