All individuals with variants in gene SLC25A15

25 entries on 1 page. Showing entries 1 - 25.
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00112540 10369256-PatHHH01 PubMed: Camacho 1999 - - - Canada French - - - - hyperornithinemia-hyperammonemia-homocitrullinemia syndrome (HHH) - 2 1 Johan den Dunnen
00112541 10369256-PatHHH011 PubMed: Camacho 1999 - - no United Kingdom (Great Britain) Japanese;Irish - - - - hyperornithinemia-hyperammonemia-homocitrullinemia syndrome (HHH) - 2 1 Johan den Dunnen
00112542 - - - M - Turkey Turkish - - - - hyperornithinemia-hyperammonemia-homocitrullinemia syndrome (HHH) 3.5y first speech problems; 6y hospitalized for first attack with severe tantrum, confusion, gait disturbances, loss of speech abilities, physical examination showed upward paralysis, aphasia, bilateral flask paralysis upper/lower extremities and deep tendon reflexes. Cranial CT, MRI, EMG and fundoscopic findings were normal; intolerance for protein-rich foods, presented hyperornithinemia, hyperammonemia, homocitrullinuria 1 1 Nagehan Ersoy Tunali
00112543 - - - F - Italy - - - - - hyperornithinemia-hyperammonemia-homocitrullinemia syndrome (HHH) - 2 1 Johan den Dunnen
00112544 - - - - - Italy - - - - - hyperornithinemia-hyperammonemia-homocitrullinemia syndrome (HHH) - 2 1 Johan den Dunnen
00112545 - - - - - United States - - - - - ? - 1 1 Johan den Dunnen
00112546 - - - - - Italy - - - - - hyperornithinemia-hyperammonemia-homocitrullinemia syndrome (HHH) - 2 1 Johan den Dunnen
00112547 - - - - - United States - - - - - ? - 1 1 Johan den Dunnen
00112548 - - - - - United States - - - - - ? - 1 1 Johan den Dunnen
00112549 - - - - - Japan - - - - - hyperornithinemia-hyperammonemia-homocitrullinemia syndrome (HHH) - 2 1 Johan den Dunnen
00112550 - PubMed: Nakajima 1988 - - - Japan - - - - - hyperornithinemia-hyperammonemia-homocitrullinemia syndrome (HHH) - 2 1 Johan den Dunnen
00112551 - - - - - Italy - - - - - hyperornithinemia-hyperammonemia-homocitrullinemia syndrome (HHH) - 2 1 Johan den Dunnen
00112552 - - - - - - - - - - - - - 1 1 Johan den Dunnen
00112553 10369256-PatA PubMed: Camacho 1999 9 unrelated probands - - Canada French - - - - hyperornithinemia-hyperammonemia-homocitrullinemia syndrome (HHH) - 1 9 Johan den Dunnen
00112554 - - - - - Italy - - - - - hyperornithinemia-hyperammonemia-homocitrullinemia syndrome (HHH) - 2 1 Johan den Dunnen
00112555 - - - - - - - - - - - - - 1 1 Johan den Dunnen
00112556 - - - - - United States - - - - - ? - 1 1 Johan den Dunnen
00112557 - - - - - United States - - - - - ? - 1 1 Johan den Dunnen
00112558 - - - - - Italy - - - - - hyperornithinemia-hyperammonemia-homocitrullinemia syndrome (HHH) - 2 1 Johan den Dunnen
00112559 - - - - - Italy - - - - - hyperornithinemia-hyperammonemia-homocitrullinemia syndrome (HHH) - 2 1 Johan den Dunnen
00112560 - - - - - Italy - - - - - hyperornithinemia-hyperammonemia-homocitrullinemia syndrome (HHH) - 2 1 Johan den Dunnen
00112561 - - - - - United States - - - - - ? - 1 2 Johan den Dunnen
00290934 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00327004 - - - M - - - - - - - ? Intellectual disability (HP:0001249); Seizure (HP:0001250); Global developmental delay (HP:0001263); Talipes equinovarus (HP:0001762); Hyperornithinemia (HP:0012026) 1 1 IMGAG
00451367 3bINP-021 PubMed: Vela-Amieva 2024 Co-occurrence of two different monogenic diseases F no Mexico Mexican - - - - hyperornithinemia-hyperammonemia-homocitrullinemia syndrome (HHH) Seizures, hyperammonemia, intellectual disability, abnormality of coagulation 1 1 Miriam Erandi Reyna-Fabián
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