All individuals with variants in gene HSD3B7

5 entries on 1 page. Showing entries 1 - 5.
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00050683 - PubMed: DDDS 2015, Journal: DDDS 2015 family, affected sibling(s) M - United Kingdom (Great Britain) - - - Decipher - ? microcephaly, abnormality of the outer ear, prominent metopic ridge, narrow mouth, inferior vermis hypoplasia, delayed speech and language development 1 2 Johan den Dunnen
00080891 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - CBAS1 Bile acid synthesis defect, congenital, 1 (OMIM:607765) 1 1 Daniel Trujillano
00307442 Fam15PatLP14 PubMed: Stalke 2018 - - - Germany - - - - - ? characteristic phenotype (Neonatal cholestasis) 1 1 Johan den Dunnen
00390025 3 PubMed: Ruberto 2020 - ? - Italy - - - - - retinal disease Pale and tilted optic disk associated to hypoplasia, tortuous retinal vessels, non-homogeneous macula 1 1 LOVD
00415276 31 PubMed: Alfares 2018 - F - - - - - - - retinal disease OMIM: 607765; cholestatic jaundice 1 1 LOVD
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