Amyloidosis

Disease Term Disease ID Gene Symbol Classification References Source
AFIB AMYLOIDOSIS
MONDO:0019733
FGA Unknown
9389696
Disgenet
AMYLOIDOSIS
C0002726MESH:D000686
TTR Causal
25595224
CTD Disgenet
ACHE Unknown
23047022
CTD Disgenet
APCS Unknown — Disgenet
APOE Unknown
15993987
CTD Disgenet
APP Unknown
23541064
CTD Disgenet
DSP Unknown — Disgenet
GOT1 Unknown — Disgenet
GSN Unknown — Disgenet
PSEN1 Unknown
23541064
CTD Disgenet
SERPINE1 Unknown — Disgenet
ZDHHC13 Unknown
20548961
CTD Disgenet
AMYLOIDOSIS CUTIS DYSCHROMIA
319635C4554601
GPNMB Unknown
29336782
Disgenet Orphanet
AMYLOIDOSIS IX
MESH:C562643
OSMR Unknown — CTD
AMYLOIDOSIS, CEREBROARTERIAL, APP-RELATED
MESH:C537944
APP Unknown
10821838 2111584
CTD
AMYLOIDOSIS, FAMILIAL
C0740340MESH:D028226
FGA Unknown
8097946 8639778
CTD Disgenet
RET Unknown
12864791
CTD Disgenet
TTR Unknown
17701470 18326041
CTD Disgenet
AMYLOIDOSIS, FAMILIAL VISCERAL
C0268389MESH:C538249
APOA1 Unknown — Disgenet
B2M Unknown — Disgenet
FGA Unknown — CTD Disgenet
LYZ Unknown — Disgenet
AMYLOIDOSIS, FINNISH TYPE
105120
GSN Unknown — HPO
AMYLOIDOSIS, HEREDITARY SYSTEMIC 1
105210MONDO:0971004
TTR Causal
25604431 28213611 15185500 30328212 15930086 9191784 29941560 32969287
ClinVar GWAS catalog HPO
AMYLOIDOSIS, HEREDITARY SYSTEMIC 2
105200
FGA Unknown — HPO
AMYLOIDOSIS, HEREDITARY SYSTEMIC 3
620657
APOA1 Unknown — HPO
AMYLOIDOSIS, HEREDITARY SYSTEMIC 5
620658C5935572MONDO:0971009
LYZ Causal — ClinVar Disgenet HPO
AMYLOIDOSIS, HEREDITARY SYSTEMIC 6
620659C5935573MONDO:0971010
B2M Causal — ClinVar Disgenet HPO
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
C2751492MESH:C567782
TTR Unknown
9717013
CTD Disgenet
AMYLOIDOSIS, PRIMARY CUTANEOUS
MESH:C562642
IL31RA Unknown — CTD
AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 1
105250C4551501MONDO:0024522
OSMR Causal
17107390 19690585 20507362 23692662 27289340
ClinVar Disgenet GWAS catalog HPO
AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 2
613955C3151404MONDO:0013502
IL31RA Causal — ClinVar Disgenet GenCC HPO
AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 3
617920C4554421MONDO:0054765
GPNMB Causal
34551863 29336782
ClinVar Disgenet GenCC HPO
ATTRV122I AMYLOIDOSIS
85451MONDO:0019441
TTR Causal
11752443 25551524
GWAS catalog Orphanet
ATTRV30M AMYLOIDOSIS
85447
TTR Unknown
18925456
Orphanet
VARIANT ABETA2M AMYLOIDOSIS
314652MONDO:0017810
B2M Unknown
22693999
GWAS catalog Orphanet