Phenotypes for disease #03909 (CLN13 (lipofuscinosis, ceroid, neuronal, type 13 (CLN-13, Kufs type)), OMIM:615362)

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AscendingPhenotype ID     

Phenotype details     

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Individual ID     
0000233298 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 - - Familial, autosomal recessive - ? 35y - - Corina-Marcela Rus 00307874
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