Phenotypes for disease #04682 (FTDALS4 (dementia, frontotemporal, and/or amyotrophic lateral sclerosis, type 4 (FTDALS-4)), OMIM:616439)

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000274622 Juvenile arthritis; abnormal gait; Regression (Neurological) - Amyotrophic lateral sclerosis Familial - - - - - LOVD 00380769
0000274671 Abnormal gait; motor neuron disease (Neurological) - TBK?1 related phenotype Familial - - - - - LOVD 00380818
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.