Disease #00964 (CMSTA2 (myasthenic syndrome, congenital, with tubular aggregates, type 2 (CMSTA-2)), OMIM:614750)

Official abbreviation CMSTA2
Name myasthenic syndrome, congenital, with tubular aggregates, type 2 (CMSTA-2)
OMIM ID 614750
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 1
Associated with 1 gene DPAGT1
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

2 entries on 1 page. Showing entries 1 - 2.
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00034428 - - - M no Netherlands white - - - neostigmine, pyridostigmine, 3,4-DAP CMSTA2 Generalized Hypotonia, myasthenia, psychomotor developmental delay, short stature, small genitals DPAGT1 DPAGT1 1 1 Anke Rietveld
00427823 Raffaella Brugnoni - - F no Italy - - - - - CMSTA2 - DPAGT1 DPAGT1 2 2 Raffaella Brugnoni
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