All individuals with variants in gene SCLT1

8 entries on 1 page. Showing entries 1 - 8.
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AscendingIndividual ID     

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VIP     

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Phenotype details     

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Panel size     

Owner     
00003131 24285566-Fam2PatIV2 PubMed: Adly 2014, Journal: Adly 2014 4-generation family, 1 affected, unaffected heterozygous carrier parents/relatives M yes Saudi Arabia Arab 00y03m - - - OFD9 severe midline cleft lip/palate, microcephaly, choanal atresia, severe coloboma, congenital heart disease (ASD, VSD), micropenis, abnormal inner ear structures; brain MRI pachygyria, absent corpus callosum; required oxygen supplementation untill 2m, severe respiratory tract infection; cardiorespiratory arrest , died at 3m 1 1 Fowzan Alkuraya
00105025 62ORG1 PubMed: de Castro-Miró 2016 - F - Argentina - - - - - retinal disease - 2 1 Marta de Castro-Miró
00301727 17DG1005 PubMed: Maddirevula 2019 2-generation family, 2 affected sibs, unaffected heterozygous carrier parents/relatives - - - - - - - - ? congenital panhypopituitarism; hormonal deficiency affecting only GH and Thyroid; same radiological abnormalities (hypoplastic anterior pituitary with shallow sella turcica ectopic posterior lobe, and hypothalamic hamartoma); no history of developmental delay or syndromic features on evaluation 1 2 Johan den Dunnen
00332122 F50‐M PubMed: Patel 2017 patient - yes Saudi Arabia - - - - - MCOP - 1 1 LOVD
00447080 CRD-671 PubMed: Weisschuh 2024 patient, no family history M - Germany - - - - - ? - 2 1 Johan den Dunnen
00447637 UD-118 PubMed: Weisschuh 2024 patient, no family history M - Germany - - - - - ? - 2 1 Johan den Dunnen
00447691 SRP-73 PubMed: Weisschuh 2024 patient, no family history M - Germany - - - - - ? - 1 1 Johan den Dunnen
00447698 SRP-763 PubMed: Weisschuh 2024 patient, no family history F - Germany - - - - - ? - 1 1 Johan den Dunnen
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