Disease #02831 (LDS1 (Loeys-Dietz syndrome, type 1 (LDS-1)), OMIM:609192)

Official abbreviation LDS1
Name Loeys-Dietz syndrome, type 1 (LDS-1)
OMIM ID 609192
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 16
Phenotype entries for this disease 13
Associated with 1 gene TGFBR1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

16 entries on 1 page. Showing entries 1 - 16.
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00133646 - - - - - - - - - - - LDS1 - FLNA FLNA 1 1 Elyssa Cannaerts
00144417 - - 3 affecteds F - Japan Asian - - - David procedure LDS1 Pectus excavatum (HP:0000767), long fingers (HP:0100807), scoliosis (HP:0002650), high palate (HP:0000218), dural ectasia (HP:0100775), ascending aortic aneurysm (HP:0002631), carotid artery tortuosity (HP:0005302), no ectopia lentis (-HP:0001083), no hypertelorism (-HP:0000316), no bifid uvula (-HP:0000193) TGFBR1 TGFBR1 1 3 Norifumi Takeda
00151836 - - - M - Japan Asian - - - - LDS1 Pectus excavatum (HP:0000767), long fingers (HP:0100807), scoliosis (HP:0002650), dural ectasia (HP:0100775), ascending aortic aneurysm (HP:0002631), hypertelorism (HP:0000316), bifid uvula (HP:0000193), Arterial tortuosity (HP:0005116), Tall stature (HP:0000098), Mitral valve prolapse (HP:0001634), no ectopia lentis (-HP:0001083) ACTA2, FBN2, MYH11, SMAD3, TGFB2, TGFB3, TGFBR1, TGFBR2 TGFBR1 1 1 Hironori Hara
00181216 - - - - - - - - - - - LDS1 - ACTA2, COL3A1, FBN1, MYH11, MYLK, SMAD3, TGFB2, TGFBR1, TGFBR2 TGFBR1 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00235309 - PubMed: Laterza 2019 - M no Italy - - - - - LDS1 - SMAD2, SMAD3, TGFB2, TGFB3, TGFBR1, TGFBR2 TGFBR1 1 1 Marco Ritelli
00245208 F1, I PubMed: Camerota 2019, Journal: Camerota 2019 - M no Italy - 07y - - - LDS1 - SMAD3, TGFB2, TGFB3, TGFBR1, TGFBR2 TGFBR1 1 1 Marco Ritelli
00245211 F2, I PubMed: Camerota 2019, Journal: Camerota 2019 - F no Italy - 31y - - - LDS1 - SMAD3, TGFB2, TGFB3, TGFBR1, TGFBR2 TGFBR1 1 2 Marco Ritelli
00245212 F3, I PubMed: Camerota 2019, Journal: Camerota 2019 - F no Italy - 29y - - - LDS1 - SMAD3, TGFB2, TGFB3, TGFBR1, TGFBR2 TGFBR1 1 1 Marco Ritelli
00245213 F4, I PubMed: Camerota 2019, Journal: Camerota 2019 patient has an affected brother carrying the same variant M no Italy - 29y - - - LDS1 - SMAD3, TGFB2, TGFB3, TGFBR1, TGFBR2 TGFBR1 1 2 Marco Ritelli
00245343 F5, I PubMed: Camerota 2019, Journal: Camerota 2019 - M no Italy - 47y - - - LDS1 - SMAD3, TGFB2, TGFB3, TGFBR1, TGFBR2 TGFBR1 1 2 Marco Ritelli
00245345 F6, I PubMed: Camerota 2019, Journal: Camerota 2019 - F no Philippines - 17y - - - LDS1 - SMAD3, TGFB2, TGFB3, TGFBR1, TGFBR2 TGFBR1 1 1 Marco Ritelli
00245346 F7, I PubMed: Camerota 2019, Journal: Camerota 2019 - M no Italy - 23y - - - LDS1 - SMAD3, TGFB2, TGFB3, TGFBR1, TGFBR2 TGFBR1 1 1 Marco Ritelli
00245347 F8, I PubMed: Camerota 2019, Journal: Camerota 2019 - M no Italy - 17y - - - LDS1 - SMAD3, TGFB2, TGFB3, TGFBR1, TGFBR2 TGFBR1 1 1 Marco Ritelli
00245348 F9, I PubMed: Camerota 2019, Journal: Camerota 2019 - M no Italy - 43y - - - LDS1 - SMAD3, TGFB2, TGFB3, TGFBR1, TGFBR2 TGFBR1 1 1 Marco Ritelli
00373331 P1 Ritelli et al., 2021 submited - F no Italy - - - - - LDS1 - TGFBR1 TGFBR1 1 2 Marco Ritelli
00373332 P3 Ritelli et al., 2021 submited - F no Italy - - - - - LDS1 - TGFBR1 TGFBR1 1 1 Marco Ritelli
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