Disease #05049 (ALS22 (sclerosis, lateral, amyotrophic, type 22 with/without frontotemoral dementia (ALS22)), OMIM:616208)

Official abbreviation ALS22
Name sclerosis, lateral, amyotrophic, type 22 with/without frontotemoral dementia (ALS22)
OMIM ID 616208
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene TUBA4A
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 11:00:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
  Powered by LOVD v.3.0 Build 30b
LOVD software ©2004-2024 Leiden University Medical Center
Database contents © by their respective submitters and curators
 There are currently no updates.