Disease #03363 (MLASA2 (myopathy, lactic acidosis, and sideroblastic anemia, type 2 (MLASA2)), OMIM:613561)

Official abbreviation MLASA2
Name myopathy, lactic acidosis, and sideroblastic anemia, type 2 (MLASA2)
OMIM ID 613561
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 1 gene YARS2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-03-19 12:45:02 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00204192 - - - - - Lebanon Lebanese - - - - MLASA2 - YARS2 TRMU, YARS2 2 1 Isabelle Thiffault
00204193 - PubMed: Riley 2010 - M yes Lebanon Lebanese - - - - MLASA2 - YARS2 YARS2 2 1 LOVD
00204194 - PubMed: Riley 2010 Sister of II:2 F yes Lebanon Lebanese - - - - MLASA2 - YARS2 YARS2 2 1 LOVD
00204196 - PubMed: Riley 2010 A maternal aunt is said to have had transfusion-dependent sideroblastic anemia and a skeletal myopathy, but never had a muscle biopsy. Brothers & sisters are healthy F yes Lebanon Lebanese - - - - MLASA2 - YARS2 YARS2 2 1 LOVD
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