Disease #00103 (Amyloidosis, Hereditary, Transthyretin-Related, OMIM:105210)

Official abbreviation -
Name Amyloidosis, Hereditary, Transthyretin-Related
OMIM ID 105210
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 6
Phenotype entries for this disease 0
Associated with 1 gene TTR
Associated tissues -
Disease features -
Remarks -


Individuals

6 entries on 1 page. Showing entries 1 - 6.
Legend   How to query  

AscendingIndividual ID     

Reference     

Gender     

Geographic origin     

Ethnic origin     

Population     

Remarks     

Microattribution     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00000560 Soon Chai Low et al.(2021) F Malaysia Chinese - - - Amyloidosis, Hereditary, Transthyretin-Related - TTR TTR 3 1 Nur Aisyah Athirah
00000561 Soon Chai Low et al.(2021) M Malaysia Chinese - - - Amyloidosis, Hereditary, Transthyretin-Related - TTR TTR 2 1 Nur Aisyah Athirah
00000562 Soon Chai Low et al.(2021) M Malaysia Malay - - - Amyloidosis, Hereditary, Transthyretin-Related - TTR TTR 1 1 Nur Aisyah Athirah
00000563 Soon Chai Low et al.(2021) F Malaysia Tamil - - - Amyloidosis, Hereditary, Transthyretin-Related - TTR TTR 1 1 Nur Aisyah Athirah
00000564 Soon Chai Low et al.(2021) M Malaysia Tamil - - - Amyloidosis, Hereditary, Transthyretin-Related - TTR TTR 1 1 Nur Aisyah Athirah
00000569 Goh Khean-Jin et al.(2008) (http://www.neurology-asia.org/articles/20082_121.pdf) M Malaysia Chinese - - - Amyloidosis, Hereditary, Transthyretin-Related - TTR TTR 1 1 Nur Aisyah Athirah
Legend   How to query