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

Official abbreviation FTDALS4
Name dementia, frontotemporal, and/or amyotrophic lateral sclerosis, type 4 (FTDALS-4)
OMIM ID 616439
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene TBK1
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:23 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00380769 ? PubMed: Nair 2018 - ? - Lebanon - - - - - FTDALS4 Juvenile arthritis; abnormal gait; Regression (Neurological) - TBK1 1 1 LOVD
00380818 ? PubMed: Nair 2018 - ? - Lebanon - - - - - FTDALS4 Abnormal gait; motor neuron disease (Neurological) - TBK1 1 1 LOVD
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