All individuals with variants in gene FLG

19 entries on 1 page. Showing entries 1 - 19.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00050174 - PubMed: Smith 2006 Frequent mutation in the European population - - United Kingdom (Great Britain) - - - - - ichthyosis vulgaris palmar hyperlinearity, keratosis pilaris 1 1 Michel van Geel
00050222 - PubMed: DDDS 2015, Journal: DDDS 2015 proband - - United Kingdom (Great Britain) - - - - - ? severe undiagnosed developmental disorders 1 1 Johan den Dunnen
00050342 - PubMed: DDDS 2015, Journal: DDDS 2015 proband - - United Kingdom (Great Britain) - - - - - ? severe undiagnosed developmental disorders 2 1 Johan den Dunnen
00050356 - PubMed: DDDS 2015, Journal: DDDS 2015 uninherited diplotypes - - United Kingdom (Great Britain) - - - - - ? severe undiagnosed developmental disorders 2 1 Johan den Dunnen
00050668 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected M - United Kingdom (Great Britain) - - - Decipher - ? global developmental delay, widely spaced teeth, depressed nasal bridge, broad-based gait, microcephaly, delayed speech and language development, eczema 2 1 Johan den Dunnen
00058555 FamPatII1/2 PubMed: Reish 2016 2-generation family, affected brother/sister, unaffected heterozygous carrier parents F;M yes Israel Bedouin - - - - HTX situs inversus (HP:0001696) 1 2 Ruti Parvari
00234470 - PubMed: Smith 2006 Frequent mutation in European population - - United Kingdom (Great Britain) - - - - - ichthyosis vulgaris - 1 1 Michel van Geel
00289524 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 3 Mohammed Faruq
00289525 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 6 Mohammed Faruq
00375227 - Nagtzaam et al, submitted patient ID 15 M - Netherlands - - - - - XLI - 2 1 Michel van Geel
00410566 Pat28 PubMed: Schuermans 2022 analysis 329 adult patients suffering from undiagnosed rare disease M - Belgium - - - - - ? see paper; ..., onset childhood, ichthyosis, no family history 2 1 Johan den Dunnen
00414411 WHP78 PubMed: Sun 2018 - F - China - - - - - ? - 2 1 LOVD
00414412 WHP79 PubMed: Sun 2018 - F - China - - - - - ? - 1 1 LOVD
00414416 WHP83 PubMed: Sun 2018 - F - China - - - - - ? - 1 1 LOVD
00414417 WHP84 PubMed: Sun 2018 - F - China - - - - - ? - 1 1 LOVD
00414418 WHP85 PubMed: Sun 2018 - F - China - - - - - ? - 1 1 LOVD
00419558 20034 PubMed: Marinakis 2021 - M - Greece - - - - - ? - 1 1 Jan Traeger-Synodinos
00437942 patient PubMed: Ferrer 2019 3-generation family, 1 triple affected F - United States - - - - - ATOD, ECTD, WITKOS see paper; ..., motor delay, speech delay, scoliosis, distinctive craniofacial features (prominent forehead, epicanthus, depressed nasal bridge, narrow mouth, prognathism, malar flattening, oligodontia), dry skin; family history dry skin mother, missing teeth paternal grandmother 1 1 Johan den Dunnen
00449695 Pat1 PubMed: van der Made 2024, Journal: van der Made 2024 2-generation family, 1 affected, unaffected non-carrier parents M - - Europe - - - - SCID see paper; ..., failure to thrive; diarrhea; <7d-skin rash; recurrent infections; no systemic inflammation; no hepatomegaly; lymphadenopathy; alopecia; dysmorphic (overfolded helices, hypoplasia alea nasi, cone-shaped teeth, hypodontia); 12w-hematopoietic stem cell transplantation 1 1 Johan den Dunnen
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.