Disease #02665 (FTLDTDP;PPA (degeneration, frontotemporal lobar, with TDP43 inclusions (FTLD-TDP, aphasia, primary progressive (PPA))), OMIM:607485)

Official abbreviation FTLDTDP;PPA
Name degeneration, frontotemporal lobar, with TDP43 inclusions (FTLD-TDP, aphasia, primary progressive (PPA))
OMIM ID 607485
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 8
Phenotype entries for this disease 1
Associated with 1 gene GRN
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

8 entries on 1 page. Showing entries 1 - 8.
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00149323 - - Basque Country - - Spain white 66y - - - ?, FTLDTDP;PPA - GRN GRN 1 4 Marc Cruts
00149601 - - - - - - - - - - - FTLDTDP;PPA - GRN GRN 1 1 Marc Cruts
00149606 - - - - - - - - - - - FTLDTDP;PPA - GRN GRN 1 1 Marc Cruts
00149608 - - - - - - - - - - - FTLDTDP;PPA - GRN GRN 1 1 Marc Cruts
00149613 - - - - - - - - - - - FTLDTDP;PPA - GRN GRN 1 1 Marc Cruts
00149614 - - - - - - - - - - - FTLDTDP;PPA - GRN GRN 1 1 Marc Cruts
00204722 - PubMed: Chiang 2012 - - - Norway - - - - - FTLDTDP;PPA - TARDBP TARDBP 1 1 Serena Lattante
00204751 - PubMed: Borghero 2011 - - - Italy - - - - - ALS, FTLDTDP;PPA - TARDBP TARDBP 1 1 Serena Lattante
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