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

Official abbreviation CTRCT-4
Name cataract, type 4 (CTRCT-4)
OMIM ID 115700
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene CRYGD
Associated tissues -
Disease features autosomal dominant
Remarks -


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00382145 191 PubMed: Patel 2019 - ? - United Kingdom (Great Britain) - - 0 - - CTRCT-4 congenital cataract; MIM, 115700 CRYGD CRYGD 1 1 LOVD
00382146 290 PubMed: Patel 2019 - ? - United Kingdom (Great Britain) - - 0 - - CTRCT-4 congenital cataract; MIM, 115700 CRYGD CRYGD 1 1 LOVD
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