Disease #01695 (Sengers;MTDPS10 (Senger syndrome (mitochondrial DNA depletion syndrome, type 10 (cardiomyopathic type, MTDPS-10))), OMIM:212350)

Official abbreviation Sengers;MTDPS10
Name Senger syndrome (mitochondrial DNA depletion syndrome, type 10 (cardiomyopathic type, MTDPS-10))
OMIM ID 212350
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene AGK
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2023-11-14 13:54:06 +01:00 (CET)


Individuals

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00409552 K6289 PubMed: Oishi 2018 - M - Japan - - - - - Sengers;MTDPS10 best corrected visual acuity: 0.5; electroretinogram , rod: n.a., cone: n.a. CYP4V2 CYP4V2 1 1 LOVD
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