Disease #00856 (MTDPS11 (mitochondrial DNA depletion syndrome, type 11 (MTDPS-11)), OMIM:615084)

Official abbreviation MTDPS11
Name mitochondrial DNA depletion syndrome, type 11 (MTDPS-11)
OMIM ID 615084
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene MGME1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00081068 - PubMed: Trujillano 2017 no information from parents - - - - - - - - MTDPS11 m DNA depletion syndrome 11 (OMIM:615084) MGME1 MGME1 1 1 Daniel Trujillano
00431386 - - - F likely Brazil - - - - - MTDPS11 - MGME1 MGME1 1 350 Eduardo Estephan
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.