Phenotypes for disease #00154 (KNO2 (Knobloch syndrome, type 2 (KNO-2)), OMIM:608454)

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AscendingPhenotype ID     

Diagnosis/Initial     

Inheritance     

Age/Examination     

Diagnosis/Definite     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Phenotype details     

Protein     

Owner     

Individual ID     
0000000656 - Isolated (sporadic) 08y - - - - after birth occipital meningocoele noted, brain CT normal; normal cognitive/motor development; 18m-poor vision; ectopia lentis, cataract (left eye), retinal degeneration, serous retinal detachment (left eye), high myopia; occipital encephalocele, developmental delay - Johan den Dunnen 00001390
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