Disease #05233 (lipodystrophy, congenital, and fatty liver disease)

Official abbreviation -
Name lipodystrophy, congenital, and fatty liver disease
OMIM ID -
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene PCYT1A
Associated tissues -
Disease features -
Remarks -
Date created 2017-03-05 16:17:19 +01:00 (CET)
Date last edited N/A


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00095896 - PubMed: Payne 2014, Journal: Payne 2014 2-generation family, 1 affected, unaffected carrier parents M no United Kingdom (Great Britain) - - - - - lipodystrophy, congenital, and fatty liver disease see paper; … BRF1, GEMIN5, PCYT1A BRF1, GEMIN5, PCYT1A 4 1 Johan den Dunnen
00095897 - PubMed: Payne 2014, Journal: Payne 2014 2-generation family, 1 affected, unaffected carrier parents F no United Kingdom (Great Britain) - - - - - lipodystrophy, congenital, and fatty liver disease see paper; … PCYT1A PCYT1A 2 1 Johan den Dunnen
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