All individuals with variants in gene SERAC1

21 entries on 1 page. Showing entries 1 - 21.
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00080949 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - MEGDEL 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome (OMIM:614739) 1 1 Daniel Trujillano
00100918 22683713-Pat1 PubMed: Wortmann 2012, Journal: Wortmann 2012 - F yes Turkey - 10y - - - MEGDEL see paper; … 1 1 Johan den Dunnen
00100919 22683713-Pat2 PubMed: Wortmann 2012, Journal: Wortmann 2012 - F no Netherlands - 16y - - - MEGDEL see paper; … 1 1 Johan den Dunnen
00100920 22683713-Pat3 PubMed: Wortmann 2012, Journal: Wortmann 2012 3-generation family, 3 affects (2F, M), niece of Pat6/7 F yes Turkey - >15y - - - MEGDEL see paper; … 1 3 Johan den Dunnen
00100921 22683713-Pat4 PubMed: Wortmann 2012, Journal: Wortmann 2012 - F yes Turkey - >15y - - - MEGDEL see paper; … 1 1 Johan den Dunnen
00100922 22683713-Pat5 PubMed: Wortmann 2012, Journal: Wortmann 2012 2-generation family, 1 affected, unaffected heterozygous carrier parents M yes Pakistan - >11y - - - MEGDEL see paper; … 1 1 Johan den Dunnen
00100923 22683713-Pat6 PubMed: Wortmann 2012, Journal: Wortmann 2012 sister of Pat7, niece of Pat3 F yes Turkey - >7y - - - MEGDEL see paper; … 1 1 Johan den Dunnen
00100924 22683713-Pat7 PubMed: Wortmann 2012, Journal: Wortmann 2012 brother of Pat6 M yes Turkey - 7d - - - MEGDEL see paper; … 1 1 Johan den Dunnen
00100925 22683713-Pat8 PubMed: Wortmann 2012, Journal: Wortmann 2012 - M yes Afghanistan - 9y - - - MEGDEL see paper; … 1 1 Johan den Dunnen
00100926 22683713-Pat9 PubMed: Wortmann 2012, Journal: Wortmann 2012 - M no Turkey - >4y - - - MEGDEL see paper; … 1 1 Johan den Dunnen
00100927 22683713-Pat10 PubMed: Wortmann 2012, Journal: Wortmann 2012 2-generation family, 1 affected, unaffected heterozygous carrier parents F no Poland - >5y - - - MEGDEL see paper; … 2 1 Johan den Dunnen
00100928 22683713-Pat11 PubMed: Wortmann 2012, Journal: Wortmann 2012 2-generation family, 1 affected, unaffected heterozygous carrier parents F no Poland - >8y - - - MEGDEL see paper; … 2 1 Johan den Dunnen
00100929 22683713-Pat12 PubMed: Wortmann 2012, Journal: Wortmann 2012 2-generation family, 1 affected, unaffected heterozygous carrier parents F no Italy - >10y - - - MEGDEL see paper; … 1 1 Johan den Dunnen
00100930 22683713-Pat13 PubMed: Wortmann 2012, Journal: Wortmann 2012 2-generation family, 1 affected, unaffected heterozygous carrier parents M no Sweden - 9y - - - MEGDEL see paper; … 2 1 Johan den Dunnen
00100931 22683713-Pat14 PubMed: Wortmann 2012, Journal: Wortmann 2012 2-generation family, 1 affected, unaffected heterozygous carrier parents M no Sweden - 15y - - - MEGDEL see paper; … 2 1 Johan den Dunnen
00100932 22683713-Pat15 PubMed: Wortmann 2012, Journal: Wortmann 2012 2-generation family, 1 affected, unaffected heterozygous carrier parents M no Sweden - 3y - - - MEGDEL see paper; … 2 1 Johan den Dunnen
00132971 - - - M - (Germany) - - - - - ? Hyperammonemia (HP:0001987); Hypokalemia (HP:0002900); Lactic acidosis (HP:0003128); 3-Methylglutaconic aciduria (HP:0003535) 1 1 IMGAG
00274171 Pat37 PubMed: Pronicka 2016 - M - Poland - - - - - ? neonatal onset; 3-MGA in urine; involvement basal ganglia; mitochondrial disease criteria score 7; muscle biopsy 1 1 Johan den Dunnen
00426154 61BN3600 PubMed: Al-Kasbi 2022 patient, other affecteds in family M - Oman - - - - - ID - 1 1 Johan den Dunnen
00426155 10BN16300 PubMed: Al-Kasbi 2022 patient, no other affecteds in family M - Oman - - - - - ID - 1 1 Johan den Dunnen
00466505 patient PubMed: Saneto 2022, Journal: Saneto 2022 - F - United States - - - - - microcephaly see paper; ..., birth hypotonia, low weight (15%), short length (5%), microcephaly (Z -9.3); moderate sensorineural hearing loss; brother 3y-deceased, ensorineural hearing loss, no expressive language, no sit, no walk 1 1 Johan den Dunnen
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