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 -
Associated with 1 gene TTR
Associated tissues -
Disease features -
Remarks -


Individuals

6 entries on 1 page. Showing entries 1 - 6.
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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
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