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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