Disease #02964 (CTCRT11;CTPP4 (cataract, type 11, multiple types (CTRCT-11, cataract, posterior polar, type 4 (CTPP-4))), OMIM:610623)

Official abbreviation CTCRT11;CTPP4
Name cataract, type 11, multiple types (CTRCT-11, cataract, posterior polar, type 4 (CTPP-4))
OMIM ID 610623
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 1 gene 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

5 entries on 1 page. Showing entries 1 - 5.
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00100419 - - - M no France - - - - - CTCRT11;CTPP4 - PITX3 PITX3 1 5 Celia Zazo-Seco
00100420 - - - F - Iraq - - - - - CTCRT11;CTPP4 - PITX3 PITX3 1 2 Celia Zazo-Seco
00100422 - - - M - England - - - - - CTCRT11;CTPP4 microphthalmia, bilateral cataract, severe autism PITX3 PITX3 1 1 Celia Zazo-Seco
00100423 - - - M ? France - - - - - CTCRT11;CTPP4 - PITX3 PITX3 1 2 Celia Zazo-Seco
00100424 - - - M - France - - - - - CTCRT11;CTPP4 - PITX3 PITX3 1 2 Celia Zazo-Seco
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