Disease #00040 (MTDPS7 (mitochondrial DNA depletion syndrome (hepatocerebral), type 7 (MTDPS-7)), OMIM:271245)

Official abbreviation MTDPS7
Name mitochondrial DNA depletion syndrome (hepatocerebral), type 7 (MTDPS-7)
OMIM ID 271245
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 7
Phenotype entries for this disease 7
Associated with 1 gene C10orf2
Associated tissues -
Disease features -
Remarks -
Date created 2012-08-30 16:45:18 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

7 entries on 1 page. Showing entries 1 - 7.
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00003014 Pat6mov PubMed: Neveling 2013 - - - - - - - - - MTDPS7 Complicated Ataxie C10orf2 C10orf2 1 1 Marcel Nelen
00060278 - Submitted for publication - F no United States - - - - - MTDPS7 - C10orf2 C10orf2 2 1 Sarah Pierce
00060281 - PubMed: Hartley 2012 2-generation family, 1 affected, unaffected heterozygous carrier parents F - Canada English >05y - - - MTDPS7 see paper; ..., infantile-onset spinocerebellar ataxia (IOSCA) C10orf2 C10orf2 2 1 Johan den Dunnen
00060282 - PubMed: Dündar 2012 6-generation family, 4 affecteds (3F, M), unaffected heterozygous carrier parents/sibs F;M yes Turkey - - - - - MTDPS7 see paper; ..., infantile onset spinocerebellar ataxia (IOSCA C10orf2 C10orf2 1 4 Johan den Dunnen
00060284 - PubMed: Nikali 2005 1 family, unaffected heterozygous carrier parents/sibs - - Finland - - - - - MTDPS7 infantile onset spinocerebellar ataxia (IOSCA) C10orf2 C10orf2 2 1 Johan den Dunnen
00060285 - PubMed: Nikali 2005 14 Finnish families, 20 patients, shared haplotype, unaffected heterozygous carriers - - Finland - - - - - MTDPS7 infantile onset spinocerebellar ataxia (IOSCA) C10orf2 C10orf2 1 20 Johan den Dunnen
00060286 - PubMed: Faruq 2013 2-generation family, affected sister/brother, unaffected heterozygous carrier parents F;M yes India - - - - - MTDPS7 infantile onset spinocerebellar ataxia (IOSCA); see paper ... C10orf2 C10orf2 1 2 Johan den Dunnen
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