Global Variome shared LOVD

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Phenotype #0000233298 Individual ID 00307874 Associated disease CLN13 Phenotype details Urinary incontinence, Dementia, Impaired social interactions, Lethargy, Mental deterioration, Hepatic steatosis, Frontotemporal cerebral atrophy, Social and occupational deterioration, Speech apraxia, Brain atrophy, Impairment of activities of daily living Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis ? Age/Onset 35y Phenotype/Onset - Protein - Owner name Corina-Marcela Rus Database submission license No license selected Created by Corina-Marcela Rus Date created 2020-08-20 02:24:37 +02:00 (CEST) Date last edited 2020-08-23 15:30:35 +02:00 (CEST)

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