Disease #00186 (MCOPS2 (microphthalmia, syndromic, type 2), OMIM:300166)

Official abbreviation MCOPS2
Name microphthalmia, syndromic, type 2
OMIM ID 300166
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene BCOR
Associated tissues -
Disease features -
Remarks -
Date created 2013-09-05 15:25:12 +02:00 (CEST)
Date last edited 2023-12-28 13:54:22 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00002450 - - radioculomegaly F no Japan - - - - - MCOPS2 - BCOR BCOR 2 1 Surapornsawasd Thunyaporn
00002451 - - radioculomegaly F no Japan - - - - - MCOPS2 - BCOR BCOR 1 1 Surapornsawasd Thunyaporn
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