Also known as: CMS21, SLC18A3 congenital myasthenic syndrome, congenital myasthenic syndrome 21, presynaptic, congenital myasthenic syndrome caused by mutation in SLC18A3, congenital myasthenic syndrome type 21, myasthenic syndrome, congenital, 21, presynaptic
Also known as: CMS IIa, CMS2A, SCCMS, congenital myasthenic syndrome 2A slow-channel, congenital myasthenic syndrome type 2A, myasthenic syndrome, congenital, 2A, slow-channel, myasthenic syndrome, congenital, postsynaptic slow-channel, myasthenic syndrome, congenital, slow-channel, myasthenic syndrome, congenital, type IIa, slow channel congenital myasthenic syndrome
Also known as: CMS2C, congenital myasthenic syndrome 2C associated with acetylcholine receptor deficiency, congenital myasthenic syndrome type 2C, myasthenic syndrome, congenital, 2C, associated with acetylcholine receptor deficiency
Also known as: CMS3A, congenital myasthenic syndrome 3A, slow-channel, congenital myasthenic syndrome type 3A, myasthenic syndrome, congenital, 3A, slow-channel
Also known as: CMS3B, congenital myasthenic syndrome 3B, fast-channel, congenital myasthenic syndrome type 3B, myasthenic syndrome, congenital, 3B, FAST-channel
Also known as: CMS3C, congenital myasthenic syndrome 3C associated with acetylcholine receptor deficiency, congenital myasthenic syndrome type 3C, myasthenic syndrome, congenital, 3C, associated with acetylcholine receptor deficiency
Also known as: CMS Ia1, CMS1A1, CMS4A, Cms Ia1, Cms Ia1, formerly, congenital myasthenic syndrome 4A slow-channel, congenital myasthenic syndrome type 4A, congenital myasthenic syndrome type Ia1, congenital myasthenic syndrome type Ia1, formerly, congenital myasthenic syndrometype Ia1, myasthenic syndrome, congenital, 4A, slow-channel
Also known as: CMS4B, congenital myasthenic syndrome 4B fast-channel, congenital myasthenic syndrome type 4B, myasthenic syndrome, congenital, 4B, FAST-channel
Also known as: CMS Id, CMS1D, CMS4C, Cms Id, Cms Id, formerly, FIM1, congenital myasthenic syndrome 4C associated with acetylcholine receptor deficiency, congenital myasthenic syndrome associated with acetylcholine receptor deficiency, congenital myasthenic syndrome type 4C, congenital myasthenic syndrome type Id, familial infantile myasthenia 1, myasthenia, familial infantile, 1, myasthenia, familial infantile, 1, formerly, myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency, myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency, myasthenic syndrome, congenital, type Id
Also known as: CMS Ic, CMS5, COLQ congenital myasthenic syndrome, Cms Ic, Cms Ic, formerly, EAD, Engel congenital myasthenic syndrome, congenital myasthenic syndrome 5, congenital myasthenic syndrome Engel type, congenital myasthenic syndrome caused by mutation in COLQ, congenital myasthenic syndrome type 5, congenital myasthenic syndrome type Ic, congenital myasthenic syndrome type Ic, formerly, end plate acetylcholinesterase deficiency, endplate acetylcholinesterase deficiency, myasthenic syndrome, congenital, 5, myasthenic syndrome, congenital, Engel type, myasthenic syndrome, congenital, type 5
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