Disease #01563 (SMAFK (atrophy, muscular, spinal, proximal, adult, autosomal dominant), OMIM:182980)

Official abbreviation SMAFK
Name atrophy, muscular, spinal, proximal, adult, autosomal dominant
OMIM ID 182980
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene VAPB
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

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00204191 - - - - - - - - - - - ALS8, SMAFK - VAPB VAPB 1 1 SIB - Livia Famiglietti
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