Global Variome shared LOVD

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Phenotype #0000288760 Individual ID 00395562 Associated disease - Phenotype details astigmatism, hypermetropia, oculomotor apraxia, photophobia, posterior subcapsular cataract, rod-cone dystrophy, intellectual disability, language impairment, dysmetria, small angioma Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite MORM (mental retardation, truncal obesity, retinal dystrophy and micropenis) syndrome Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2021-12-08 14:12:08 +01:00 (CET) Date last edited N/A

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