Disease #01232 (CTRCT4 (cataract, type 4 (CTRCT-4)), OMIM:115700)

Official abbreviation CTRCT4
Name cataract, type 4 (CTRCT-4)
OMIM ID 115700
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene CRYGD
Associated tissues -
Disease features autosomal dominant
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

3 entries on 1 page. Showing entries 1 - 3.
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00382145 191 PubMed: Patel 2019 - ? - United Kingdom (Great Britain) - - - - - CTRCT4 congenital cataract; MIM, 115700 CRYGD CRYGD 1 1 LOVD
00382146 290 PubMed: Patel 2019 - ? - United Kingdom (Great Britain) - - - - - CTRCT4 congenital cataract; MIM, 115700 CRYGD CRYGD 1 1 LOVD
00412325 199902 - - F no Germany - - - - - CTRCT4 Developmental cataract, Episodic ataxia, Vertigo, Reduced visual acuity; many affected family members CRYGD CRYGD 1 1 Andreas Laner
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