Disease #00042 (MTDPS3 (mitochondrial DNA depletion syndrome (hepatocerebral), type 3 (MTDPS-3)), OMIM:251880)

Official abbreviation MTDPS3
Name mitochondrial DNA depletion syndrome (hepatocerebral), type 3 (MTDPS-3)
OMIM ID 251880
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 DGUOK
Associated tissues -
Disease features -
Remarks -
Date created 2012-08-30 16:46:44 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00004534 - - - - no - - - - - - MTDPS3 - DGUOK DGUOK 2 1 Carl Fratter
00004535 - - - - - - - - - - - MTDPS3 - DGUOK DGUOK 1 1 Carl Fratter
00081031 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - MTDPS3 m DNA depletion syndrome 3 (hepatocerebral type) (OMIM:251880) DGUOK DGUOK, DGUOK-AS1 1 1 Daniel Trujillano
00081059 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - MTDPS3 m DNA depletion syndrome 3 (hepatocerebral type) (OMIM:251880) DGUOK DGUOK, DGUOK-AS1 1 1 Daniel Trujillano
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