Phenotypes for disease #03570 (BCS2 (cornea, brittle, syndrome type 2 (BCS-2)), OMIM:614170)

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AscendingPhenotype ID     

Phenotype details     

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Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

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Individual ID     
0000038135 see paper, brittel cornea syndrome, ... - - Familial, autosomal recessive - - - - - Shazia Micheal 00051532
0000337264 see paper; ..., marked corneal thinning, irregular astigmatism, characteristic sclerae, arachnodactyly, joint laxity, particularly large joints upper extremities, pes planus brittle cornea syndrome BCS2 Familial, autosomal recessive 09y - - - - Johan den Dunnen 00038385
0000337265 see paper; ..., blue sclera, significant corneal thinning, high myopia with choroidal neovascularization, scoliosis, arachnodactyly, joint hypermobility brittle cornea syndrome BCS2 Familial, autosomal recessive - - - - - Johan den Dunnen 00038386
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