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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