Disease #01235 (CTRCT1 (cataract, type 1 (CTRCT1)), OMIM:116200)

Official abbreviation CTRCT1
Name cataract, type 1 (CTRCT1)
OMIM ID 116200
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 7
Phenotype entries for this disease 7
Associated with 1 gene GJA8
Associated tissues -
Disease features -
Remarks -


Individuals

7 entries on 1 page. Showing entries 1 - 7.
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00060073 - - - - - United Kingdom (Great Britain) - - 0 - - CTRCT1 - GJA8 GJA8 1 1 Johan den Dunnen
00060074 - - - - - Pakistan - - 0 - - CTRCT1 - GJA8 GJA8 1 1 Johan den Dunnen
00060075 - - - - - Russian Federation - - 0 - - CTRCT1 - GJA8 GJA8 1 1 Johan den Dunnen
00060077 - - - - - India - - 0 - - CTRCT1 - GJA8 GJA8 1 1 Johan den Dunnen
00060078 - - - - - - - - 0 - - CTRCT1 - GJA8 GJA8 1 1 Johan den Dunnen
00060079 - - - - - China - - 0 - - CTRCT1 - GJA8 GJA8 1 1 Johan den Dunnen
00384435 14525 PubMed: Wang 2019 - F - China - - 0 - - CTRCT1 - GJA8 GJA8 1 1 LOVD
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