Global Variome shared LOVD

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Phenotype #0000245867 Individual ID 00327622 Associated disease ? Diagnosis/Initial - Diagnosis/Definite - Phenotype details Rod-cone dystrophy (HP:0000510); Hypothyroidism (HP:0000821); Global developmental delay (HP:0001263); Congenital stationary night blindness (HP:0007642); Schizophrenia (HP:0100753) Inheritance Unknown Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name IMGAG Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by IMGAG Date created 2021-01-25 10:38:01 +01:00 (CET) Date last edited 2021-01-29 09:16:48 +01:00 (CET)

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