Disease #00322 (MTDPS5 (mitochondrial DNA depletion syndrome, type 5 (MTDPS-5, encephalomyopathic with/without methylmalonic aciduria)), OMIM:612073)

Official abbreviation MTDPS5
Name mitochondrial DNA depletion syndrome, type 5 (MTDPS-5, encephalomyopathic with/without methylmalonic aciduria)
OMIM ID 612073
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 SUCLA2
Associated tissues -
Disease features -
Remarks -
Date created 2014-02-02 22:41:39 +01:00 (CET)
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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00004541 - - - M yes United Kingdom (Great Britain) Pakistani - - - - MTDPS5 - SUCLA2 SUCLA2 1 1 Robert McFarland
00016594 - - - - - - - - - - - MTDPS5 - SUCLA2 SUCLA2 1 1 Sanna Matilainen
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