Disease #04639 (CMS11 (myasthenic syndrome, congenital, type 11, associated with acetylcholine receptor deficiency (CMS-11)), OMIM:616326)

Official abbreviation CMS11
Name myasthenic syndrome, congenital, type 11, associated with acetylcholine receptor deficiency (CMS-11)
OMIM ID 616326
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 5
Phenotype entries for this disease 2
Associated with 1 gene RAPSN
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:23 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00406616 1 - - F - - - - - - - CMS11 - - RAPSN 1 1 Martin Krenn
00406655 25 - - M - - - - - - - CMS11 - - RAPSN 2 1 Martin Krenn
00415980 - - unaffected heterozygous parents M no Argentina - - - - pyridostigmine CMS11 HP:0000276 Long face HP:0000218 High palate HP:0000508 Ptosis HP:0000338 Hypomimic face HP:0001252 Hypotonia HP:0002098 Respiratory distress (neonatal) HP:0003388 Easy fatigability HP:0002650 Scoliosis (mild) HP:0001558 Decreased fetal movement HP:0001388 Joint laxity Positive response to pyridostigmine - RAPSN 2 1 María Eugenia Foncuberta
00415999 - - unaffected heterozygous parents M no Argentina - - - - pyridostigmine CMS11 HP:0000431 Wide nasal bridge HP:0001252 Hypotonia HP:0000508 Ptosis HP:0000276 Long face HP:0000218 High palate HP:0001558 Decreased fetal movement HP:0001324 Muscle weakness retraction of Achilles positive response to pyridostigmine - RAPSN 2 1 María Eugenia Foncuberta
00424147 - - - - - Netherlands - - - - - CMS11 - RAPSN RAPSN 2 1 Erik-Jan Kamsteeg
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