Disease #03907 (LGMDR18;LGMD2S (dystrophy, muscular, limb-girdle, autosomal recessive, type 18 (LGMD2S)), OMIM:615356)

Official abbreviation LGMDR18;LGMD2S
Name dystrophy, muscular, limb-girdle, autosomal recessive, type 18 (LGMD2S)
OMIM ID 615356
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 TRAPPC11
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2023-10-24 15:18:22 +02:00 (CEST)


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00111404 S_081 PubMed: Popp 2017, Journal: Popp 2017 - F no - - - - - - LGMDR18;LGMD2S Strabismus, mildly elevated CK, moderate ID, movement disorder TRAPPC11 TRAPPC11 1 1 Bernt Popp
00119098 - - - M no United Kingdom (Great Britain) Chinese - - - - LGMDR18;LGMD2S early onset limb girdle muscular dystrophy (HP:0006785); walk-22m, muscular pseudohypertrophy (HP:0003707), proximal weakness (HP:0003701), bilateral cataracts (HP:0000519), normal cognition (no ntellectual disability, HP:0001249) - TRAPPC11 2 1 Nadine McCrea
00446904 - - - F no - - - - - - LGMDR18;LGMD2S - - TRAPPC11 2 1 Jana Zidkova
00446905 - - - M - - - - - - - LGMDR18;LGMD2S - - TRAPPC11 2 1 Jana Zidkova
00446906 - - - M - - - - - - - LGMDR18;LGMD2S - - TRAPPC11 2 1 Jana Zidkova
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