Disease #03706 (ALS17 (sclerosis, lateral, amyotrophic, type 17 (ALS17)), OMIM:614696)

Official abbreviation ALS17
Name sclerosis, lateral, amyotrophic, type 17 (ALS17)
OMIM ID 614696
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 4
Phenotype entries for this disease -
Associated with 1 gene CHMP2B
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

4 entries on 1 page. Showing entries 1 - 4.
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00149650 - - - - - United Kingdom (Great Britain) white 55y - - - ALS17 - CHMP2B CHMP2B 1 1 Marc Cruts
00149679 - - - - - - - 70y - - - ALS17 - CHMP2B CHMP2B 1 1 Marc Cruts
00149680 - - - - - - - 52y - - - ALS17 - CHMP2B CHMP2B 1 1 Marc Cruts
00149681 - - - - - - - 74y - - - ALS17 - CHMP2B CHMP2B 1 1 Marc Cruts
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